{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/at/fortrea/"},"x-facet":{"type":"company","slug":"fortrea","display":"Fortrea","count":100},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_55f51c5c-f77"},"title":"Site Budget Specialist","description":"<p>Join Fortrea and shape the future of clinical research! As a Site Budget Specialist, you will play a critical role in the clinical trials budgeting process, driving the success of groundbreaking studies while ensuring compliance and efficiency.</p>\n<p>In this role, you will be part of the FSPx team and work directly with a renowned key sponsor to advance the development of innovative, life-changing medications.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Support Country Study site budget template, parameter, and payment term building to ensure timely setup of individual site budgets.</li>\n<li>Manage and execute assigned study site budget maintenance activities throughout the study lifecycle.</li>\n<li>Negotiate directly with globally assigned sites on master clinical trial agreements rate cards.</li>\n<li>Partner with the site payment department to ensure site budget and payment terms compatibility with payment systems and EDC requirements.</li>\n<li>Collaborate with internal Study Startup teams, Clinical Operations teams, and TAU partners to improve overall SB&amp;C metrics and implement processes.</li>\n<li>Ensure standards are applied to SB&amp;C processes across projects and portfolios, supporting continuous improvement activities while developing TA-aligned strategies.</li>\n<li>Leverage leading industry tools and data sources to provide budget and payment terms feedback aligned with parameters and fair market value guidance.</li>\n<li>Promptly recognise and improve potential delays, escalating non-performance.</li>\n</ul>\n<p><strong>Required Qualifications:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree (LLB, JD, BA, or BS) preferred; 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Toronto/CRA-1-2---Sr-CRAs---Oncology---General-Medicine--French-Speaking-Desired--Canada_263916","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Toronto/CRA-1-2---Sr-CRAs---Oncology---General-Medicine--French-Speaking-Desired--Canada_263916","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Clinical Monitoring","Oncology","Ophthalmology","French"],"x-skills-preferred":["CAR-T 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and oversight across non-clinic early-phase delivery models.</li>\n<li>Ensure alignment with Clinical Operations, Medical, and Safety.</li>\n<li>Embed quality-by-design principles into early-phase program design and execution.</li>\n<li>Provide executive oversight of compliance risks, escalation, and remediation strategies across CPS and early-phase programs.</li>\n<li>Ensure adherence to RC&amp;QA governance requirements and controlled documentation.</li>\n<li>Serve as delegate within the RC&amp;QA Leadership Team and contribute to enterprise governance forums.</li>\n<li>Partner with CPS and enterprise leadership to drive quality culture and execution.</li>\n<li>Influence strategic priorities and resource allocation aligned with CPS and early-phase delivery.</li>\n<li>Represent Fortrea externally as an SME in clinical pharmacology, GMP pharmacy oversight, and early-phase quality.</li>\n<li>Communicate quality strategy effectively to internal and external stakeholders.</li>\n<li>Lead 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of formal education.</li>\n<li>Proven ability to define and execute QA strategies in clinical pharmacology, CPU operations, and GMP-controlled environments.</li>\n<li>Experience overseeing pharmacy operations supporting clinical trials (IP management under GMP).</li>\n<li>Demonstrated success leading global, matrixed teams.</li>\n<li>Strong executive presence with ability to influence internal and external stakeholders.</li>\n<li>Experience implementing risk-based quality oversight for early-phase trials.</li>\n<li>Strong track record in inspection readiness and regulatory engagement.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment</strong></p>\n<ul>\n<li>Ideally located at one of the Fortrea CPS units (Madison, WI - Dallas, TX - Daytona Beach, FL - Leeds, United Kingdom).</li>\n<li>Travel to CPUs, GMP pharmacies, and global sites as required.</li>\n<li>Flexibility for extended hours aligned with business and inspection needs.</li>\n</ul>\n<p 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contact for investigative sites and ensure timely delivery in alignment with scope of work/study budget</li>\n<li>Perform Case Report Form (CRF) review and data validation against source documentation</li>\n<li>Perform country and site ICF review/customization, per local requirements</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution</li>\n<li>3+ years&#39; work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations</li>\n<li>Fluent in local official language and in English, both written and verbal</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>A scientific degree and/ or clinical expertise is optimal for this role</li>\n<li>Minimum of 2 +year of experience in clinical development or start-up/ regulatory process</li>\n<li>Working knowledge of 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-CRA_25113","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-CRA_25113","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":null,"x-salary-range":null,"x-skills-required":["clinical trials","monitoring experience","complexity management","communication skills","stakeholder 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You will lead a team and be accountable for quality oversight and management, resource management, and financial delivery. 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profitability goals</li>\n<li>Identify business opportunities within country through proactive networking with customer stakeholders</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>University/college degree in life sciences or certification in a related allied health profession</li>\n<li>Expert level of English and local language required</li>\n<li>Thorough knowledge of drug development process and relevant SOPs, ICH, and GCP guidelines</li>\n<li>Ability to manage a team to ICH GCP/FDA/ISO14155 standards</li>\n<li>Demonstrated ability to lead by example and encourage team members to be responsible and accountable</li>\n<li>Excellent planning and organisational skills</li>\n<li>Strong financial acumen</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>Minimum of 10 years supervisory experience, including 2 years of managing managers</li>\n<li>1 year leading a team or function with 4 years experience of effectively managing customer relationships in a healthcare or clinical research setting</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Senior-Director--Clinical-Network_263685","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Senior-Director--Clinical-Network_263685","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["life sciences","clinical operations","leadership","financial management","quality management"],"x-skills-preferred":["Masters or other advanced degree"],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-07-02T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Tokyo"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"life sciences, clinical operations, leadership, financial management, quality management, Masters or other advanced degree"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_7c4e7bf6-43d"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to manage and monitor clinical studies at various sites.</p>\n<p>The successful candidate will be responsible for ensuring that studies are conducted in accordance with Company and Sponsor Standard Operating Procedures, as well as Regulatory Guidelines.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Conducting routine monitoring and closeout of clinical sites</li>\n<li>Maintaining study files and conducting pre-study and initiation visits</li>\n<li>Liaising with vendors and other stakeholders</li>\n<li>Ensuring that study staff have received proper materials and instructions to safely enter patients into the study</li>\n<li>Verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Reviewing data for missing or implausible entries</li>\n<li>Ensuring audit readiness at the site level</li>\n<li>Preparing accurate and timely trip reports</li>\n<li>Interacting with internal work groups to evaluate needs, resources, and timelines</li>\n<li>Acting as a contact for clinical trial supplies and other suppliers</li>\n<li>Managing investigator site budgets</li>\n<li>Tracking and following up on Serious Adverse Event reporting</li>\n<li>Performing CRF review and query generation</li>\n<li>Assisting with training and 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Chengdu/FSP-CRA-I-II-Hefei-_256018","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Chengdu/FSP-CRA-I-II-Hefei-_256018","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial management","regulatory guidelines","monitoring","data analysis","communication"],"x-skills-preferred":["clinical operations","medical terminology","CTMS","customer service"],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T20:29:59.205Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Chengdu"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial management, regulatory guidelines, monitoring, data analysis, communication, clinical operations, medical terminology, CTMS, customer service"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_cf4f71b0-8b6"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.</p>\n<p>The successful candidate will be responsible for:</p>\n<ul>\n<li>Conducting site monitoring responsibilities for clinical trials, including pre-study, site initiation, process monitoring, routine monitoring, and close-out visits</li>\n<li>Preparing and implementing project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensuring the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguarding data integrity through source document review, source document verification, query generation, and resolution</li>\n<li>Confirming site regulatory documents and eTMF/Sponsor documents are complete and current</li>\n<li>Guaranteeing the accuracy of Investigational Product inventory and accountability</li>\n<li>Ensuring adherence to global quality control and CRA performance metrics</li>\n<li>Ensuring audit readiness at site level</li>\n<li>Acting as a Lead CRA as assigned</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A university or college degree, or certification in a related allied health profession</li>\n<li>Thorough understanding of ICH GCP Guidelines and local regulatory requirements</li>\n<li>Knowledge of monitoring procedures and the clinical trial process</li>\n<li>Fluent in local office language and English</li>\n<li>At least 2 years of Clinical Monitoring experience</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>Additional years of experience in a related field</li>\n<li>Phase I monitoring experience</li>\n<li>Life Science or Nursing qualification</li>\n</ul>\n<p>The role involves travel, including air travel, which is an essential function of the job. The ability to work with minimal supervision and have good planning, organization, and problem-solving abilities is required.</p>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Must be able to sit at a computer for long periods</li>\n<li>Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment (administrative only)</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours as required by the role</li>\n<li>Travel Requirement is 60% of the time (travelling to study sites)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a 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establishing succession plans for key resources</li>\n<li>Preparing and delivering presentations for new business as required</li>\n<li>Performing other duties as assigned by management</li>\n</ul>\n<p>You will also be responsible for line management and talent development, including training and mentoring project managers, assessing project management competencies, and providing line management and technical support to assigned project leaders.</p>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>University/college degree (life science preferred) or certification in a related allied health profession</li>\n<li>Minimum of seven years of relevant clinical research experience in a pharmaceutical company/CRO, including at least two years of full project management responsibility</li>\n<li>Working knowledge of ICH Guidelines and GCP, including international regulatory requirements for the conduct of clinical development programs</li>\n<li>Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and PowerPoint)</li>\n<li>Experience managing projects in a matrix and virtual environment</li>\n<li>Excellent communication, planning, and organisational skills</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Master&#39;s or other advanced degree</li>\n<li>PMP certification</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Senior-Project-Manager_263317","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Senior-Project-Manager_263317","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH Guidelines","GCP","Microsoft Office","project 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The successful candidate will maintain and contribute to contracts tracking and status systems, support the maintenance of paper and electronic file systems, and ensure adherence to standard operating procedures (SOPs).</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Prepare, negotiate, and execute site agreements, confidentiality agreements, and other contracts</li>\n<li>Maintain and update contracts tracking and status systems</li>\n<li>Ensure compliance with SOPs and internal processes</li>\n<li>Identify and escalate issues to line managers as necessary</li>\n<li>Manage assigned studies and ensure timely updating of contract tracking systems</li>\n<li>Perform contract administration functions, including obtaining approvals and maintaining contract records</li>\n<li>Support line managers with departmental goals and initiatives</li>\n<li>Provide regular status updates on open contracts and outstanding issues</li>\n<li>Draft, negotiate, review, and process contracts in a commercially reasonable manner</li>\n<li>Apply knowledge of ICH GCP principles and quality standard procedures</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>Bachelor&#39;s degree (LLB, JD, BA or BS) preferred; university-level law degree preferred (UK/EU)</li>\n<li>Relevant and equivalent experience in lieu of educational requirements may be considered</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Minimum 2-4 years of experience, or an equivalent combination of education and experience</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>100% office environment</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Contract-Assoc-II_263608","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Tokyo/Contract-Assoc-II_263608","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP","contract negotiation","contract management","SOPs"],"x-skills-preferred":["university-level law degree","relevant experience"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-07-06T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Tokyo"}},"employmentType":"FULL_TIME","occupationalCategory":"Legal","industry":"Consulting","skills":"ICH GCP, contract negotiation, contract management, SOPs, university-level law degree, relevant experience"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_711d93ba-f0b"},"title":"Senior CRA I","description":"<p>The Senior CRA I is responsible for site monitoring and site management. You will be responsible for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines.</p>\n<p>You will assure the implementation of project plans, as assigned, and function as leader for projects of limited scope. You may also assume line management responsibilities and act in the project role of a Local Project Coordinator or Lead CRA.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conduct site monitoring, including routine monitoring and closeout of clinical sites, maintenance of study files, and pre-study and initiation visits</li>\n<li>Liaise with vendors and perform other duties as assigned</li>\n<li>Ensure study staff have received proper materials and instructions to safely enter patients into the study</li>\n<li>Verify informed consent procedures and protocol requirements are adhered to according to regulatory requirements</li>\n<li>Review source documents to ensure data integrity</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Manage travel expenses in an economical fashion according to Fortrea&#39;s travel policy</li>\n<li>Prepare accurate and timely trip reports</li>\n<li>Manage small projects under the direction of a Project Manager/Director</li>\n<li>Serve as lead monitor for a protocol or project</li>\n<li>Participate in protocol development and writing clinical trial reports</li>\n<li>Interact with internal work groups to evaluate needs, resources, and timelines</li>\n<li>Act as contact for clinical trial supplies and other suppliers</li>\n<li>Undertake feasibility work and conduct Quality Control visits</li>\n<li>Recruit potential investigators, prepare EC submissions, and notify regulatory authorities</li>\n<li>Negotiate study budgets with potential investigators</li>\n<li>Track and follow-up on Serious Adverse Event reporting</li>\n<li>Independently perform CRF review and query generation</li>\n<li>Assist with training and mentoring new employees</li>\n<li>Coordinate designated clinical projects as a Local Project Coordinator</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University or college degree in life sciences or related field, or certification in a related allied health profession</li>\n<li>3 years of relevant clinical research experience in pharmaceutical or CRO industries</li>\n<li>Thorough knowledge of regulatory requirements and drug development process</li>\n<li>Fluent in local office language and English</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>3 years of Clinical Monitoring experience</li>\n<li>Advanced site monitoring, study site management, and registry administration skills</li>\n<li>Ability to work with minimal supervision and good planning and organisation skills</li>\n<li>Good computer skills and advanced verbal and written communication skills</li>\n<li>Ability to train and supervise junior staff</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Travel requirements: 60-80% overnight</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Shanghai/FSP-SCRA-I--Harbin--Changchun--Shenyang-_263556","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Shanghai/FSP-SCRA-I--Harbin--Changchun--Shenyang-_263556","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","site monitoring","study management","regulatory requirements","drug development process","English"],"x-skills-preferred":["local project coordination","project management"],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-07-13T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Shanghai"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical research, site monitoring, study management, regulatory requirements, drug development process, English, local project coordination, project management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ed82bf1a-a44"},"title":"Clinical Research Associate (CRA)","description":"<p>Work Across Cutting-Edge Science That Truly Makes a Difference</p>\n<p>What if your CRA role exposed you to some of the most exciting and meaningful science in clinical research?</p>\n<p>At Fortrea, our CRAs don’t sit in narrow silos. You’ll work across a diverse and challenging portfolio that reflects where medicine is going, not where it’s been.</p>\n<p>Our study portfolio includes:</p>\n<ul>\n<li>Oncology</li>\n<li>Neuroscience</li>\n<li>General Medicine</li>\n<li>Cell &amp; Gene Therapy</li>\n<li>CAR-T Therapy Studies</li>\n</ul>\n<p>This means real complexity, real learning, and the chance to build a profile that sets you apart as a CRA.</p>\n<p>Why CRAs choose us:</p>\n<ul>\n<li>Breadth of experience – develop expertise across multiple therapeutic areas</li>\n<li>Exposure to advanced therapies – cell &amp; gene, CAR-T, innovative trial designs</li>\n<li>Supportive leadership – managers who understand the demands of complex studies</li>\n<li>Career acceleration – skills that open doors, not limit them</li>\n<li>A culture of trust – autonomy, collaboration, and respect for your expertise</li>\n</ul>\n<p>If you’re a CRA who enjoys scientific challenge, values quality over box-ticking, and wants to feel proud of the studies you support - this could be your next move!</p>\n<p>The role:</p>\n<ul>\n<li>Lead and manage sites across varied and complex indications</li>\n<li>Build trusted relationships with investigators and study teams</li>\n<li>Ensure patient safety and data integrity remain paramount</li>\n<li>Contribute actively to innovative and first-in-class studies</li>\n</ul>\n<p>We’re looking for:</p>\n<ul>\n<li>Monitoring experience in clinical trials</li>\n<li>Curiosity and comfort with complexity</li>\n<li>Strong communication and stakeholder skills</li>\n<li>A desire to grow your portfolio and your career</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/CRA-II_254567","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/CRA-II_254567","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trials","monitoring experience","complexity management","communication skills","stakeholder management"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-05-06T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Maidenhead"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trials, monitoring experience, complexity management, communication skills, stakeholder management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c248c985-b0a"},"title":"Senior Biostatistician","description":"<p>Fortrea is looking for a Senior Biostatistician to join our sponsor-dedicated team.</p>\n<p>As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.</p>\n<p><strong>Your Responsibilities:</strong></p>\n<ul>\n<li>Design and implement statistical strategies for clinical trials within various therapeutic areas.</li>\n<li>Develop statistical analysis plans, ensuring their appropriateness for study objectives.</li>\n<li>Perform statistical programming tasks using SAS for analyses and generate study reports.</li>\n<li>Collaborate with cross-functional study teams to contribute statistical expertise and guidance.</li>\n<li>Provide expertise on statistical methodology, sample size calculations, and innovative trial design.</li>\n<li>Ensure the quality and integrity of statistical deliverables.</li>\n<li>Oversight of all the statistical queries on multiple projects.</li>\n</ul>\n<p><strong>Your experience and qualifications:</strong></p>\n<ul>\n<li>Minimum of 5 years of experience as a Biostatistician within a CRO, biotech or pharmaceutical company.</li>\n<li>Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.</li>\n<li>Extensive knowledge of CDISC standards.</li>\n<li>Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs.</li>\n<li>Proven professional experience with SDTMs, ADaM datasets and TFLs.</li>\n<li>Strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards.</li>\n<li>Excellent communication skills, with the ability to effectively collaborate and present complex data to non-technical audiences.</li>\n<li>Advanced degree (Ph.D. or Master’s) in Biostatistics, Statistics, or a related field.</li>\n<li>Demonstrated ability to work independently, utilize problem-solving skills, and make sound decisions.</li>\n</ul>\n<p><strong>What you can expect from us:</strong></p>\n<ul>\n<li>Pioneering Research: Join a CRO at the forefront of clinical trials within multiple therapeutic areas.</li>\n<li>Career Growth: Expand your skill set and broaden your expertise in a supportive environment, with numerous opportunities for career advancement.</li>\n<li>Impactful Work: Contribute directly to the development of groundbreaking therapies and treatments, improving the lives of patients worldwide.</li>\n<li>Competitive Compensation: We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure.</li>\n<li>Life-Style: Flexibility to work remotely from anywhere, promoting a healthy work-life balance.</li>\n</ul>\n<p>You can be 100% home-based in any of the EMEA locations.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Biostatistician_262353","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://www.fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Biostatistician_262353","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Biostatistics","Statistical Analysis","SAS","CDISC standards","Clinical Trials","Regulatory Guidelines"],"x-skills-preferred":[],"x-benefits":["bonus"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-05-08T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"Biostatistics, Statistical Analysis, SAS, CDISC standards, Clinical Trials, Regulatory Guidelines"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_277afd88-26e"},"title":"Clinical Research Associate II (CRA2)","description":"<p>We&#39;re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.</p>\n<p>As a CRA2, you will play a key role in managing and monitoring clinical trials, ensuring compliance with regulatory requirements, and fostering strong relationships with investigative sites. This is a fantastic opportunity for professionals looking to grow their career in a dynamic and collaborative environment.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Site management responsibility for clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.</li>\n<li>Conducts site monitoring responsibilities for clinical trials according to Fortrea&#39;s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.</li>\n<li>Prepares and implements project plans related to Clinical Monitoring responsibilities.</li>\n<li>Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.</li>\n<li>Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.</li>\n<li>Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.</li>\n<li>Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.</li>\n<li>Ensures adherence to global quality control and CRA performance metrics.</li>\n<li>Ensures audit readiness at site level.</li>\n<li>Acts in the project role of a Lead CRA as assigned.</li>\n</ul>\n<p><strong>General On-Site Monitoring Responsibilities:</strong></p>\n<ul>\n<li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study.</li>\n<li>Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.</li>\n<li>Ensure the integrity of the source data reported by careful source document review.</li>\n<li>Monitor data for missing or implausible data.</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.</li>\n<li>Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines.</li>\n<li>Travel, including air travel, may be required and is an essential function of the job.</li>\n<li>Prepare and submit accurate and timely trip reports.</li>\n<li>Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.</li>\n<li>Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management.</li>\n<li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.</li>\n<li>Track IP shipments and supplies, as needed.</li>\n<li>Track and follow-up on serious adverse events as assigned.</li>\n<li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.</li>\n<li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.</li>\n<li>Attend investigators&#39; meetings, project team meetings and teleconferences, and others as needed.</li>\n<li>Present training content for site initiation.</li>\n<li>Assist with training of new employees.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution.</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.</li>\n<li>Thorough knowledge of monitoring procedures.</li>\n<li>Basic understanding of the clinical trial process.</li>\n<li>Fluent in local office language and in English, both written and verbal.</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Typically 2 years of onsite clinical site monitoring experience.</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.</li>\n<li>Ability to work with minimal supervision.</li>\n<li>Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.</li>\n<li>Good planning, organization, and problem-solving abilities.</li>\n<li>Works efficiently and effectively in a matrix environment.</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Location: Incumbent of the role needs to be based in Sydney and happy to work 3 days from the office if not travelling.</li>\n<li>Will involve outside of normal office hours as required by the role.</li>\n<li>Travel Requirement is 60% of the time.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Clinical-Research-Associate-II---Sydney_261587","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Clinical-Research-Associate-II---Sydney_261587","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","clinical trial management","site monitoring","data integrity","regulatory compliance","English"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-05-05T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sydney"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, clinical trial management, site monitoring, data integrity, regulatory compliance, English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_0bc50b6c-f7c"},"title":"Contracts Coordinator","description":"<p>We are seeking a Contracts Coordinator to prepare and negotiate site agreements, confidentiality agreements, and other contracts for sponsors. The successful candidate will maintain and contribute to contracts tracking and status systems, support the maintenance of paper and electronic file systems, and ensure adherence to standard operating procedures (SOPs).</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Prepare, negotiate, and execute site agreements, confidentiality agreements, and other contracts</li>\n<li>Maintain and update contracts tracking and status systems</li>\n<li>Ensure compliance with internal processes and procedures, as well as sponsor requirements</li>\n<li>Identify and escalate issues to line managers for review</li>\n<li>Confirm quality of tasks delegated to and completed by Contracts Associates</li>\n<li>Manage assigned studies with careful compliance with internal processes and procedures</li>\n<li>Perform contract administration functions, including obtaining approvals and maintaining a contract tracking system</li>\n<li>Provide regular status updates on all open contracts and outstanding issues</li>\n<li>Support line managers with departmental goals, objectives, and initiatives</li>\n<li>Draft, negotiate, review, and process contracts in a commercially reasonable manner</li>\n<li>Negotiate contractual terms with other contracting parties</li>\n<li>Apply knowledge of ICH GCP principles and follow quality standard procedures</li>\n<li>Identify potential obstacles in the contracting process and request assistance as necessary</li>\n<li>Work closely with staff to keep them informed of progress and avoid delays</li>\n<li>Provide support to other Site Agreements staff and assist internal staff with contractual inquiries</li>\n<li>Facilitate internal review and revision of contracts</li>\n<li>Coordinate and communicate with clinical study teams regarding contract details and timelines</li>\n<li>Assist in development and ongoing improvement of departmental processes and procedures</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>Bachelor&#39;s degree (LLB, JD, BA or BS) preferred; university-level law degree preferred (UK/EU)</li>\n<li>Relevant and equivalent experience in lieu of educational requirements may be considered</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Minimum 2-4 years of experience, or an equivalent combination of education and experience</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>100% office environment</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Mexico/Contracts-Spec-II_262258","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Mexico/Contracts-Spec-II_262258","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP","contract negotiation","contract administration","SOPs"],"x-skills-preferred":["university-level law degree","relevant experience"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-05-05T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote Mexico"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Legal","industry":"Consulting","skills":"ICH GCP, contract negotiation, contract administration, SOPs, university-level law degree, relevant experience"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c55f7bf5-47e"},"title":"Clinical Research Registered Nurse - Early Phase Clinical Trials (Multiple Shifts Available)","description":"<p>We are seeking a dedicated Clinical Research Registered Nurse to support the execution of innovative Early Phase clinical trials, ensuring participant safety and protocol accuracy.</p>\n<p>This role is ideal for nurses who prefer rotating shifts, mid shift or night work, value schedule transparency, and thrive in a focused clinical research environment.</p>\n<p><strong>Schedule Options:</strong></p>\n<ul>\n<li>Option 1: Rotating Shift: 10-hour shifts, rotating weekends to include a 12-hour shift</li>\n<li>Option 2: Mid Shift: 10-hour shifts, start time between 11am and 1pm, rotating weekends to include a 12-hour shift</li>\n<li>Option 3: Night Shift: Monday–Friday: 10‑hour shifts, 9pm - 7:30am, rotating weekends to include a 12-hour shift (7pm - 7:30am)</li>\n</ul>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Deliver high-quality care to trial participants using clinical judgment and nursing expertise</li>\n<li>Monitor participant well-being, document adverse events, and respond to emergencies</li>\n<li>Administer investigational compounds and perform study-related procedures (ECGs, telemetry, venipuncture, etc.)</li>\n<li>Collect and process biological samples, maintain accurate records, and ensure compliance with protocols</li>\n<li>Other duties as assigned</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Associate’s or BS degree in Nursing with current state licensure</li>\n<li>CPR/AED/ACLS certification</li>\n<li>2–3 years of related experience</li>\n<li>Phlebotomy experience</li>\n<li>Registered Nurse</li>\n</ul>\n<p><strong>Benefits:</strong></p>\n<ul>\n<li>Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)</li>\n<li>401(K)</li>\n<li>Paid time off (PTO)</li>\n<li>Employee recognition awards</li>\n<li>Multiple ERG’s (employee resource groups)</li>\n</ul>\n<p><strong>Work Environment:</strong></p>\n<ul>\n<li>Laboratory and/or clinical environment with exposure to electrical office equipment</li>\n<li>Occasional drives to site locations, occasional domestic travel</li>\n<li>Exposure to biological fluids</li>\n<li>Personal protective equipment required</li>\n</ul>\n<p><strong>Physical Requirements:</strong></p>\n<ul>\n<li>Ability to work in an upright and /or stationary position for 10-12 hours per day</li>\n<li>Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment</li>\n<li>Occasional crouching, stooping, with frequent bending and twisting of upper body and neck</li>\n<li>Ability to access and use a variety of computer software</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Daytona-Beach/Clinical-Research-Registered-Nurse--Early-Phase-Clinical-Trials---Daytona-Beach--FL_261966","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Daytona-Beach/Clinical-Research-Registered-Nurse--Early-Phase-Clinical-Trials---Daytona-Beach--FL_261966","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Clinical Research","Nursing","Phlebotomy","CPR/AED/ACLS certification"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance","dental","paid_leave"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-23T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Daytona Beach, FL"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Research, Nursing, Phlebotomy, CPR/AED/ACLS certification"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b2974fbc-32c"},"title":"Site Navigators II","description":"<p>Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required.</p>\n<p>Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation, extending through the maintenance phase of the study as required.</p>\n<p>A crucial component in meeting the requirements of the Site Navigator II role is ensuring regulatory compliance, robust site management, optimal site support and training, and effective collaboration between the sponsor, CRO, and clinical site staff.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs and project requirements</li>\n<li>Identifying potential research sites that align with the study&#39;s criteria and assessing their capabilities and resources</li>\n<li>Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and feasibility survey</li>\n<li>Remote Pre-Study Visits and follow up documentation</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials</li>\n<li>Collect, track and perform a quality review of all essential documents required for effective and compliant study site activation</li>\n<li>Actively participate in team meetings to facilitate study progress and implement action plans for site level risks</li>\n<li>Support the CRA team in preparing for site initiation visits (SIVs)</li>\n<li>Responsible for submissions to and liaise with applicable IRB/IEC, Third Bodies (if applicable), and Regulatory Authorities</li>\n<li>Perform initial contract and budget negotiations with the sites</li>\n<li>Ensure high quality documents are filed in applicable systems in accordance with SOPs and project requirements</li>\n<li>Track the progress of the start-up process and ensure that the research site meets all requirements and deadlines</li>\n<li>Ensure Fortrea is audit ready by completing accurate, timely, and consistent system compliance on an ongoing basis</li>\n<li>Serve as primary contact for investigative sites and ensure timely delivery in alignment with scope of work/study budget</li>\n<li>Perform Case Report Form (CRF) review and data validation against source documentation</li>\n<li>Perform country and site ICF review/customization, per local requirements</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution</li>\n<li>3+ years&#39; work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations</li>\n<li>Fluent in local official language and in English, both written and verbal</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>A scientific degree and/ or clinical expertise is optimal for this role</li>\n<li>Minimum of 2+ years of experience in clinical start-up/ regulatory process (RGO and Ethics submissions)</li>\n<li>Working knowledge of ICH/GCP, RA, TGA, Belberry, and other applicable regulations/guidelines</li>\n<li>Demonstrated understanding of research protocol requirements and proven ability to communicate and educate others about them</li>\n<li>Effective communication with various stakeholders, including site staff, CRO personnel, and regulatory authorities</li>\n<li>Ability to manage multiple tasks and deadlines simultaneously</li>\n<li>Understanding of relevant regulations and guidelines related to clinical trials and research</li>\n<li>Ability to identify and resolve potential issues that may arise during the start-up process</li>\n<li>Ability to negotiate contracts and budgets effectively with research sites</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location</li>\n<li>Travel requirements: Limited for training only</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Australia/Site-Navigator-II--Study-Start-up-Specialist----Brisbane--Perth--Adelaide_264645","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Australia/Site-Navigator-II--Study-Start-up-Specialist----Brisbane--Perth--Adelaide_264645","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH/GCP guidelines","RA","IRB/IEC regulations","clinical research","site management","regulatory compliance"],"x-skills-preferred":["scientific degree","clinical expertise","TGA","Belberry"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-24T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote Australia"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH/GCP guidelines, RA, IRB/IEC regulations, clinical research, site management, regulatory compliance, scientific degree, clinical expertise, TGA, Belberry"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_0164d51b-c86"},"title":"Paramedic","description":"<p>We are currently seeking a Paramedic to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types.</p>\n<p>This is a full-time, office/clinic-based job in Madison, WI. Multiple shifts available.</p>\n<p>If you join us, you will work with some of the world&#39;s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Under the direction and medical oversight of the Physician/Investigator, the Paramedic serves as a primary safety contact for study participants within a Fortrea Clinical Research Unit (CRU). This role monitors participant safety and well-being, provides basic and advanced medical care within defined scope of practice, and supports protocol-required clinical activities.</p>\n<ul>\n<li>Collaborate clearly and effectively with physicians, nurses, investigators, and other clinical team members to support coordinated participant care.</li>\n<li>Deliver basic and advanced medical care, within defined scope of practice, to study participants in emergent and non-emergent situations.</li>\n<li>Lead resuscitation and stabilization efforts for participants experiencing life-threatening situations, following accepted medical protocols and study-specific treatment requirements.</li>\n<li>Monitor, document, and review active adverse events; communicate significant findings to the investigator and support ongoing safety assessments.</li>\n<li>Escalate participant safety concerns to the investigator for review and determination regarding study procedures and/or dosing.</li>\n<li>Administer medications and treatments as prescribed by the investigator or physician and in accordance with study protocols, Standing Orders, and site procedures.</li>\n<li>Perform technical procedures as delegated, including blood collection, vital sign measurement, ECGs, and other protocol-required clinical activities.</li>\n<li>Assess participants with out-of-range values for associated signs or symptoms, initiate appropriate interventions within scope of practice, and promptly notify the investigator when clinically indicated.</li>\n<li>Conduct study-related activities in accordance with study protocols, investigator instructions, Standing Orders, applicable regulations, Good Clinical Practice (GCP), Fortrea policies, and standard operating procedures.</li>\n<li>Accurately and contemporaneously document study procedures, participant observations, adverse events, interventions, and other required data in source documents and applicable systems.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>High school diploma, secondary school diploma, or equivalent required.</li>\n<li>Relevant formal academic or vocational qualification required.</li>\n<li>State license or certification as a Paramedic required.</li>\n<li>Advanced Cardiac Life Support (ACLS) certification required.</li>\n<li>Strong paramedic skills required, including airway management, IV establishment, and subcutaneous injections.</li>\n<li>Strong verbal and written communication skills with the ability to communicate professionally and credibly with staff, management, physicians, investigators, and study participants.</li>\n<li>Ability to manage multiple complex tasks and respond effectively to emergency medical situations.</li>\n<li>Previous experience that provides the knowledge, skills, and abilities to perform the job required; preferably 2 or more years of experience as a Paramedic.</li>\n<li>Experience assessing and responding to emergent and non-emergent medical situations required.</li>\n<li>Experience documenting clinical observations, interventions, adverse events, and related source data preferred.</li>\n</ul>\n<p><strong>Benefits</strong></p>\n<ul>\n<li>Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)</li>\n<li>401(K)</li>\n<li>Paid time off (PTO)</li>\n<li>Employee recognition awards</li>\n<li>Multiple ERG&#39;s (employee resource groups)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madison/Paramedic---Madison--WI--On-Site-_265382","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madison/Paramedic---Madison--WI--On-Site-_265382","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Paramedic","ACLS","clinical research","Good Clinical Practice (GCP)"],"x-skills-preferred":["experience working in a clinical research setting","knowledge of study protocols","site standard operating procedures"],"x-benefits":["pension","health_insurance","dental","paid_leave"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-16T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Madison, WI"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Paramedic, ACLS, clinical research, Good Clinical Practice (GCP), experience working in a clinical research setting, knowledge of study protocols, site standard operating procedures"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8835caff-8fe"},"title":"Senior Clinical Research Associate I","description":"<p>As a Senior Clinical Research Associate I at Fortrea, you will play a pivotal role in ensuring the success of clinical trials by managing and monitoring study sites.</p>\n<p>You’ll work closely with investigators and sponsors to uphold regulatory standards and deliver high-quality data that advances medical breakthroughs.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.</li>\n<li>Ensure patient safety and compliance with informed consent and protocol requirements.</li>\n<li>Review source documents and verify data integrity on Case Report Forms (CRFs).</li>\n<li>Prepare accurate and timely monitoring reports and maintain study files.</li>\n<li>Serve as lead monitor for assigned protocols and assist in developing monitoring plans.</li>\n<li>Coordinate with vendors and internal teams to meet project timelines and objectives.</li>\n<li>Support feasibility assessments, budget negotiations, and regulatory submissions.</li>\n<li>Mentor and train junior team members through co-monitoring and guidance.</li>\n<li>Travel extensively (60–80%) to support site activities and maintain audit readiness.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or related field, or equivalent clinical research experience.</li>\n<li>Typically a minimum of 3 years clinical onsite monitoring experience in pharmaceutical or CRO settings.</li>\n<li>Strong knowledge of regulatory requirements and drug development processes.</li>\n<li>Advanced site management skills.</li>\n<li>Excellent communication, organisational, and problem-solving abilities.</li>\n<li>Proficiency in relevant computer applications and systems.</li>\n<li>Valid driver’s license and ability to travel extensively.</li>\n<li>Have the rights to work in Australia. Sorry, no visa sponsorship support offered at this time.</li>\n</ul>\n<p><strong>Why Join Fortrea?</strong></p>\n<ul>\n<li>Contribute to groundbreaking research that improves lives worldwide.</li>\n<li>Access robust training, mentorship, and advancement opportunities.</li>\n<li>Thrive in a collaborative, inclusive environment that values work-life balance.</li>\n<li>Be part of a forward-thinking organisation shaping the future of clinical trials.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Senior-Clinical-Research-Associate-I--SCRA1----Sydney--Melbourne--Perth--Adelaide-or-Brisbane_261645-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Senior-Clinical-Research-Associate-I--SCRA1----Sydney--Melbourne--Perth--Adelaide-or-Brisbane_261645-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","regulatory requirements","drug development processes","site management","communication","organisational","problem-solving"],"x-skills-preferred":[],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"not_offered","x-visa-sponsorship-text":"Sorry, no visa sponsorship support offered at this time.","x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-24T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Sydney"}},"employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"clinical research, regulatory requirements, drug development processes, site management, communication, organisational, problem-solving"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_cecd84f7-651"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to take on site monitoring and site management responsibilities for clinical studies. You will ensure the implementation of project plans, monitor study sites, and liaise with vendors.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conduct routine monitoring and closeout of clinical sites</li>\n<li>Maintain study files and conduct pre-study and initiation visits</li>\n<li>Liaise with vendors and other stakeholders</li>\n<li>Ensure study staff have received proper materials and instructions</li>\n<li>Verify informed consent procedures and protocol requirements</li>\n<li>Review data for missing or implausible entries</li>\n<li>Monitor data quality and ensure audit readiness</li>\n<li>Travel to sites and prepare trip reports</li>\n<li>Interact with internal work groups and external suppliers</li>\n<li>Manage investigator site budgets and track Serious Adverse Events</li>\n<li>Perform CRF review and query generation</li>\n<li>Assist with training and mentoring new employees</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University or college degree in a related field (e.g., nursing, life sciences)</li>\n<li>Basic knowledge of Regulatory Guidelines and clinical trial processes</li>\n<li>Fluent in local office language and English</li>\n<li>6 months experience in a related role (e.g., site management, study coordinator)</li>\n<li>Valid Driver&#39;s License</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Additional experience in a related field (e.g., medical, clinical, pharmaceutical)</li>\n<li>On-site monitoring experience</li>\n<li>Understanding of medical and clinical research terminology</li>\n<li>Experience using a clinical trial management system (CTMS)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Guangzhou/FSP-CRA-I--Nanning-Fuzhou-Xiamen-_265593","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Guangzhou/FSP-CRA-I--Nanning-Fuzhou-Xiamen-_265593","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trials","regulatory guidelines","site management","data monitoring"],"x-skills-preferred":["CTMS","medical terminology","customer service"],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-24T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Guangzhou"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trials, regulatory guidelines, site management, data monitoring, CTMS, medical terminology, customer service"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9b148f11-764"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.</p>\n<p>The successful candidate will be responsible for:</p>\n<ul>\n<li>Conducting site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Preparing and implementing project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensuring the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguarding data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines</li>\n<li>Confirming Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial</li>\n<li>Guaranteeing that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements</li>\n<li>Ensuring adherence to global quality control and CRA performance metrics</li>\n<li>Ensuring audit readiness at site level</li>\n<li>Acting in the project role of a Lead CRA as assigned</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A university or college degree, or certification in a related allied health profession from an appropriately accredited institution</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements</li>\n<li>Thorough knowledge of monitoring procedures</li>\n<li>Basic understanding of the clinical trial process</li>\n<li>Fluent in local office language and in English, both written and verbal</li>\n<li>A minimum of 2 years of Clinical Monitoring experience</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines</li>\n<li>Ability to work with minimal supervision</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>One (1) or more additional years of experience in a related field</li>\n<li>Phase I monitoring experience</li>\n<li>Life Science or Nursing qualification</li>\n<li>Specific skills, systems, certifications, and/or licenses</li>\n<li>Good attention to detail, methodical approach to work, and good understanding of medical and clinical research terminology</li>\n</ul>\n<p>In return, we offer a competitive salary and benefits package.</p>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Must be able to sit at a computer for long periods of time</li>\n<li>Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment (administrative only)</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours as required by the role</li>\n<li>Travel Requirement is 60% of the time (travelling to study sites)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Shanghai/FSP-CRA-II--Zhengzhou-_265303","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Shanghai/FSP-CRA-II--Zhengzhou-_265303","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Clinical Monitoring","Source Document Review","Data Integrity","Regulatory Compliance"],"x-skills-preferred":["Fortrea SOPs","Phase I monitoring","Life Science or Nursing qualification","e-clinical systems"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-24T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Shanghai"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, Clinical Monitoring, Source Document Review, Data Integrity, Regulatory Compliance, Fortrea SOPs, Phase I monitoring, Life Science or Nursing qualification, e-clinical systems"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_5b4f4666-e3b"},"title":"Clinical Research Associate II (CRA2)","description":"<p>We&#39;re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.</p>\n<p>As a CRA2, you will play a key role in managing and monitoring clinical trials, ensuring compliance with regulatory requirements, and fostering strong relationships with investigative sites. This is a fantastic opportunity for professionals looking to grow their career in a dynamic and collaborative environment.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Site management responsibility for clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.</li>\n<li>Conducts site monitoring responsibilities for clinical trials according to Fortrea&#39;s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.</li>\n<li>Prepares and implements project plans related to Clinical Monitoring responsibilities.</li>\n<li>Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.</li>\n<li>Safeguards data integrity by 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or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.</li>\n<li>Ensure the integrity of the source data reported by careful source document review.</li>\n<li>Monitor data for missing or implausible data.</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.</li>\n<li>Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines.</li>\n<li>Travel, including air travel, may be required and is an essential function of the job.</li>\n<li>Prepare and submit accurate and timely trip reports.</li>\n<li>Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.</li>\n<li>Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management.</li>\n<li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.</li>\n<li>Track IP shipments and supplies, as needed.</li>\n<li>Track and follow-up on serious adverse events as assigned.</li>\n<li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.</li>\n<li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.</li>\n<li>Attend investigators&#39; meetings, project team meetings and teleconferences, and others as needed.</li>\n<li>Present training content for site initiation.</li>\n<li>Assist with training of new employees.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution.</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.</li>\n<li>Thorough knowledge of monitoring procedures.</li>\n<li>Basic understanding of the clinical trial process.</li>\n<li>Fluent in local office language and in English, both written and verbal.</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Typically 2 years of onsite clinical site monitoring experience.</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.</li>\n<li>Ability to work with minimal supervision.</li>\n<li>Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.</li>\n<li>Good planning, organization, and problem-solving abilities.</li>\n<li>Works efficiently and effectively in a matrix environment.</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Location: Incumbent of the role needs to be based in Sydney and happy to work 3 days from the office if not travelling.</li>\n<li>Will involve outside of normal office hours as required by the role.</li>\n<li>Travel Requirement is 60% of the time.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Clinical-Research-Associate-II--FSP----Sydney_265613","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Clinical-Research-Associate-II--FSP----Sydney_265613","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","clinical trial management","site monitoring","data 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experience.</p>\n<p><strong>Why Join Fortrea?</strong></p>\n<ul>\n<li>Be part of a global, innovative organisation driving advancements in clinical research.</li>\n<li>Work on cutting-edge trials across a range of therapeutic areas.</li>\n<li>Enjoy flexible career progression, with opportunities at different CRA levels.</li>\n<li>Benefit from a collaborative team environment that values mentorship and growth.</li>\n</ul>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.</li>\n<li>Manage all aspects of site activities, including site initiation, monitoring visits, and closeouts.</li>\n<li>Ensure patient safety, data integrity, and adherence to Good Clinical Practice (GCP) guidelines.</li>\n<li>Support feasibility assessments, investigator recruitment, and vendor coordination.</li>\n<li>Mentor junior team members and contribute to quality control efforts.</li>\n<li>Track and report Serious Adverse Events (SAEs) as required.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/college degree in life sciences or a relevant allied health field.</li>\n<li>At least 2 years of experience in a related role (e.g., Site Management, CRA).</li>\n<li>Phase I patient-study experience.</li>\n<li>Basic knowledge of Regulatory Guidelines and the clinical trial process.</li>\n<li>Strong communication, organisational, and problem-solving skills.</li>\n<li>A valid driver’s license and willingness to travel.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/CRA-II--client-dedicated_261833","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/CRA-II--client-dedicated_261833","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","life sciences","regulatory guidelines","clinical trial process","communication","organisational","problem-solving"],"x-skills-preferred":["Phase I patient-study experience","Site Management","CRA"],"x-benefits":[],"x-licences":["Driving 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As a Senior Clinical Research Associate, you will utilise your skills, knowledge, and clinical judgement to provide high-quality care for participants in clinical trials and respond to emergency situations based on clinical research standards.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Conduct routine monitoring and close-out of clinical sites, maintaining study files, and liaising with vendors</li>\n<li>Ensure study staff receive proper materials and instructions to safely enter patients into the study</li>\n<li>Verify informed consent procedures and protocol requirements are adhered to according to regulatory requirements</li>\n<li>Monitor data for missing or implausible data and ensure the integrity of data submitted on Case Report Forms</li>\n<li>Complete Serious Adverse Event reporting and process production of reports and narratives</li>\n<li>Independently perform CRF review, query generation, and resolution against established data review guidelines</li>\n<li>Assist with training new employees and coordinate designated clinical projects as a Local Project Coordinator</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession</li>\n<li>5+ years of Clinical Monitoring experience</li>\n<li>Oncology experience, preferably in early-phase studies</li>\n<li>Ability to travel 30-50% of the time, potentially overnight</li>\n</ul>\n<p><strong>Work Environment</strong></p>\n<ul>\n<li>Fast-paced environment with changing priorities and constant adaptation</li>\n<li>Teamwork and people skills essential for smooth study execution</li>\n<li>Technology-based, collecting data directly into an electronic environment</li>\n</ul>\n<p><strong>Physical Requirements</strong></p>\n<ul>\n<li>Ability to sit for extended periods, operate a vehicle safely, and perform repetitive hand movements</li>\n<li>Occasional crouching, stooping, bending, and twisting of upper body and neck</li>\n<li>Light to moderate lifting and carrying of objects up to 15-20 lbs</li>\n</ul>\n<p><strong>Salary</strong>: $125 - $140K</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP-Sr-Clinical-Research-Associate-II---Midwest---Oncology_265612","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP-Sr-Clinical-Research-Associate-II---Midwest---Oncology_265612","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$125 - $140K","x-skills-required":["Clinical Monitoring","Oncology","Clinical Trials","Data 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deliverables, timelines, and results, contributes to local SOPs development.</li>\n<li>Collaboration: works closely with internal teams, vendors, sites, IRB/IECs, and regulatory authorities to ensure country deliverables are met.</li>\n<li>Local process oversight: responsible for clinical and ancillary supplies management, importing and exporting requirements, and insurance process management.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>University/college degree in life sciences or a related field, or certification in a related allied health profession.</li>\n<li>Minimum 4-6 years of clinical research experience in the pharmaceutical or CRO industry.</li>\n<li>Thorough knowledge of ICH guidelines and GCP, including regulatory requirements in other countries.</li>\n<li>Fluent in French and English, both written and verbal.</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Good organisational and time management skills.</li>\n<li>Working knowledge of ICH, FDA, local regulatory requirements, and IRB/IEC regulations.</li>\n<li>Excellent communication skills, oral and written.</li>\n<li>Self-motivated with the ability to work under pressure to meet deadlines.</li>\n<li>Detail-oriented and process-oriented.</li>\n<li>Positive attitude and approach.</li>\n<li>Ability to interact with internal and external customers with a high degree of professionalism and discretion.</li>\n<li>Multi-tasking capability.</li>\n<li>Good computer skills with a range of computer packages.</li>\n<li>Ability to lead and develop junior staff.</li>\n<li>Flexible and adaptable to a developing work environment.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Montreal/Clinical-Operations-Manager--COM-_264999","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Montreal/Clinical-Operations-Manager--COM-_264999","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH guidelines","GCP","regulatory compliance","financial management","clinical trial operations","French","English"],"x-skills-preferred":["organisational skills","time management","communication 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Buenos-Aires/Sr-CRA-I_265634","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Buenos-Aires/Sr-CRA-I_265634","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","site monitoring","study management","regulatory guidelines","data integrity","communication skills"],"x-skills-preferred":["local project coordination","project management"],"x-benefits":[],"x-licences":["Driving licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-28T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Buenos Aires"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical research, site monitoring, study management, regulatory guidelines, data integrity, communication skills, local project coordination, project management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ad5828ec-a03"},"title":"On-Call Clinical Call Center Representative","description":"<p>Fortrea is hiring On-Call Clinical Call Center Representatives to support the recruitment of volunteer participants for Phase 1 healthy volunteer clinical research studies.</p>\n<p>This is a great opportunity for someone with strong customer service and communication skills who is interested in healthcare, clinical research, or gaining experience within the pharmaceutical and clinical research industry.</p>\n<p>You will be one of the first points of contact for potential study participants, helping them understand available research opportunities, completing initial phone screenings, and scheduling qualified individuals for screening appointments.</p>\n<p><strong>Work Arrangement</strong></p>\n<ul>\n<li>First week: Full-time onsite training at our Dallas, TX or Daytona Beach, FL location.</li>\n<li>After training: The position becomes fully remote.</li>\n<li>This is an on-call position, with hours scheduled according to business and recruitment needs.</li>\n<li>Candidates should have flexibility to support varying hours, which may include evenings and weekends.</li>\n<li>Pay rate: $18.00/hour.</li>\n</ul>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Handle inbound and outbound calls with individuals interested in participating in clinical research studies.</li>\n<li>Explain study opportunities and provide participants with relevant study information.</li>\n<li>Conduct initial phone screenings using study-specific scripts and guidelines.</li>\n<li>Collect and accurately enter participant demographic and medical history information into computerized systems.</li>\n<li>Schedule qualified participants for screening appointments.</li>\n<li>Confirm upcoming screening appointments and communicate next steps.</li>\n<li>Respond professionally to participant questions and inquiries.</li>\n<li>Work closely with the screening team to coordinate participant recruitment activities and required information.</li>\n<li>Maintain a high degree of accuracy, professionalism, confidentiality, and customer service.</li>\n<li>Identify opportunities to improve recruitment and participant communication processes.</li>\n<li>Perform other recruitment-related responsibilities as needed.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>High school diploma or equivalent required.</li>\n<li>1-2 years of customer service, call center, or similar customer-facing experience preferred.</li>\n<li>Strong verbal and written communication skills.</li>\n<li>Comfortable speaking with people over the phone and following structured screening scripts.</li>\n<li>Strong computer skills and ability to learn new systems quickly.</li>\n<li>Excellent attention to detail and accuracy when entering information.</li>\n<li>Professional, customer-focused approach.</li>\n<li>Ability to work independently in a remote environment following completion of training.</li>\n<li>Flexibility to work varying hours based on business needs, including potential evenings and weekends.</li>\n<li>Healthcare or medical terminology knowledge is a plus, but not required.</li>\n<li>Bilingual English/Spanish skills are a plus, but not required.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Dallas/Clinical-Call-Representative--on-call-_265457","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Dallas/Clinical-Call-Representative--on-call-_265457","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":"$18.00/hour","x-skills-required":["customer service","communication","phone screening","data entry","scheduling"],"x-skills-preferred":["Spanish","healthcare or medical terminology"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dallas, TX"}},"occupationalCategory":"Customer Service","industry":"Healthcare","skills":"customer service, communication, phone screening, data entry, scheduling, Spanish, healthcare or medical terminology"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_a573df72-724"},"title":"Regulatory Affairs Specialist","description":"<p>We are seeking a Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will serve as the primary contact with investigative sites during study maintenance and site startup activities. You will be responsible for collecting required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within agreed timelines.</p>\n<p>Your main responsibilities will include:</p>\n<ul>\n<li>Developing awareness of regulatory legislation, guidance, and practice in assigned countries with senior staff support</li>\n<li>Assisting senior staff in compiling, preparing, submitting, and obtaining approval of submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements</li>\n<li>Liaising with internal and external vendors for Regulatory Authority submissions</li>\n<li>Reviewing final submission documents as applicable</li>\n<li>Organising communication related to submissions/outcomes within Fortrea</li>\n<li>Escalating study issues in a timely fashion</li>\n</ul>\n<p>Additionally, you will perform country-specific tasks such as:</p>\n<ul>\n<li>Serving as primary contact for investigative sites and ensuring timely collection of required documents</li>\n<li>Collecting and tracking necessary documents, performing quality reviews, formatting, and compiling final documents for site activation and maintenance</li>\n<li>Ensuring all assigned maintenance and start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality, and applicable laws and guidelines</li>\n</ul>\n<p>You will also support CTIS tasks, including uploading submission documentation to CTIS under supervision.</p>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/College degree (life science preferred), or certification in a related allied health profession from an accredited institution</li>\n<li>Minimum 0-2+ years of experience, or an equivalent combination of education and experience</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines</li>\n<li>Basic understanding of the clinical trial process</li>\n</ul>\n<p><strong>Work Environment:</strong></p>\n<ul>\n<li>General Office Environment</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/Startup-Associate_265709","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/Startup-Associate_265709","x-work-arrangement":null,"x-experience-level":"entry","x-job-type":null,"x-salary-range":null,"x-skills-required":["ICH","RA","IRB/IEC","clinical trials"],"x-skills-preferred":["regulatory affairs","life science"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"São Paulo"}},"occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH, RA, IRB/IEC, clinical trials, regulatory affairs, life science"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_adfcf04a-e23"},"title":"Director of Platform Engineering","description":"<p>We are seeking a Director of Platform Engineering to lead our transformation toward a modern engineering platform. You will drive adoption of AI-assisted software engineering, cloud-native architectures, Internal Developer Platforms (IDPs), DevSecOps, Site Reliability Engineering (SRE), Infrastructure as Code (IaC), GitOps, and intelligent automation practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Support and execute Fortrea&#39;s Platform Engineering, DevOps, Cloud Engineering, and Software Delivery strategy aligned with business and technology objectives.</li>\n<li>Build, lead, mentor, and develop Engineering Managers, Platform Engineers, DevOps Engineers, Site Reliability Engineers, Cloud Engineers, and technical leaders.</li>\n<li>Establish and evolve Internal Developer Platforms (IDPs), reusable engineering services, self-service developer capabilities, golden paths, engineering templates, and developer portals.</li>\n<li>Treat engineering platforms as products by partnering with engineering teams, measuring platform adoption, collecting customer feedback, and continuously improving platform capabilities.</li>\n<li>Lead enterprise adoption of AI-assisted software engineering tools and intelligent automation.</li>\n<li>Evaluate emerging AI technologies including coding assistants, AI agents, autonomous remediation, predictive operations, and intelligent engineering platforms.</li>\n<li>Drive enterprise engineering modernization through cloud-native architectures, Kubernetes, containers, GitOps, Infrastructure as Code, CI/CD, DevSecOps, automation-first engineering practices, and platform engineering.</li>\n<li>Establish enterprise standards for CI/CD pipelines, Infrastructure as Code, release automation, cloud operations, configuration management, deployment automation, and engineering governance.</li>\n<li>Build scalable cloud platforms supporting modern software delivery using Microsoft Azure, Kubernetes, serverless technologies, API management, and cloud-native services.</li>\n<li>Establish Site Reliability Engineering (SRE) practices including Service Level Objectives (SLOs), Service Level Indicators (SLIs), error budgets, operational readiness reviews, reliability engineering, and resilience frameworks.</li>\n<li>Drive enterprise adoption of DevSecOps practices including security-by-design, software supply chain security, secrets management, automated compliance, vulnerability management, SBOM generation, and secure software delivery.</li>\n<li>Champion Developer Experience (DevEx) initiatives through self-service engineering platforms, engineering automation, developer tooling, standardized environments, and streamlined software delivery workflows.</li>\n<li>Support observability initiatives including OpenTelemetry, monitoring, logging, tracing, alerting, telemetry, dashboards, operational intelligence, and application performance monitoring.</li>\n<li>Implement AIOps capabilities leveraging machine learning and intelligent automation for anomaly detection, predictive monitoring, automated incident correlation, root cause analysis, and operational insights.</li>\n<li>Define and monitor engineering performance using DORA Metrics, SPACE Framework principles, deployment frequency, lead time for change, change failure rate, mean time to recovery (MTTR), platform adoption, developer productivity, availability, and service health metrics.</li>\n<li>Partner with Architecture teams to establish scalable, secure, API-first, cloud-native technology platforms that support Fortrea&#39;s long-term engineering strategy.</li>\n<li>Collaborate with Product Engineering, Security, Infrastructure, Data &amp; AI, Architecture, and Technology Leadership to support engineering strategy, investment priorities, platform roadmaps, and modernization initiatives.</li>\n<li>Drive cloud governance, FinOps practices, infrastructure optimization, capacity planning, cost management, and operational efficiency.</li>\n<li>Lead workforce planning, organizational design, talent acquisition, succession planning, leadership development, and continuous learning across the Platform Engineering organization.</li>\n<li>Manage engineering budgets, technology investments, strategic vendor partnerships, resource planning, and platform lifecycle management.</li>\n<li>Foster a high-performance engineering culture centered on ownership, innovation, automation-first thinking, operational excellence, engineering quality, experimentation, collaboration, continuous improvement, and customer outcomes.</li>\n<li>Continuously evaluate emerging technologies, AI capabilities, engineering platforms, cloud services, and automation opportunities that improve software delivery and operational excellence.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in Computer Science, Information Technology, Engineering, or related discipline.</li>\n<li>Advanced knowledge of Platform Engineering, DevOps, Cloud Engineering, Site Reliability Engineering (SRE), Software Delivery, and modern engineering practices.</li>\n<li>Strong understanding of cloud-native architectures, distributed systems, Kubernetes, containers, Infrastructure as Code, GitOps, CI/CD, and enterprise software engineering.</li>\n<li>Strong knowledge of Microsoft Azure and modern cloud engineering practices, with familiarity across AWS and Google Cloud Platform.</li>\n<li>Deep understanding of DevSecOps, cloud security, secure software development lifecycle, compliance automation, software supply chain security, and operational governance.</li>\n<li>Demonstrated success leading enterprise engineering transformations and building high-performing engineering organizations.</li>\n<li>Exceptional leadership, communication, organizational development, stakeholder management, and executive influencing skills.</li>\n<li>Ability to define long-term engineering strategy while delivering measurable business outcomes.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Director--Platform-Engineering---Dev-Ops_265714","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Director--Platform-Engineering---Dev-Ops_265714","x-work-arrangement":"hybrid","x-experience-level":"executive","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Platform Engineering","DevOps","Cloud Engineering","Site Reliability Engineering (SRE)","Software Delivery","Kubernetes","containers","Infrastructure as Code","GitOps","CI/CD","DevSecOps","Microsoft Azure","cloud-native architectures","distributed systems","AI-assisted software engineering","intelligent automation"],"x-skills-preferred":["GitHub Copilot Enterprise","GitHub Models","Cursor","Claude Code","Windsurf","ChatGPT Enterprise","Azure OpenAI","OpenAI APIs","Anthropic Claude","Google Vertex AI","Azure AI Services","Model Context Protocol (MCP)","Retrieval-Augmented Generation (RAG)","prompt engineering","Responsible AI","AI governance","enterprise AI security"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Platform Engineering, DevOps, Cloud Engineering, Site Reliability Engineering (SRE), Software Delivery, Kubernetes, containers, Infrastructure as Code, GitOps, CI/CD, DevSecOps, Microsoft Azure, cloud-native architectures, distributed systems, AI-assisted software engineering, intelligent automation, GitHub Copilot Enterprise, GitHub Models, Cursor, Claude Code, Windsurf, ChatGPT Enterprise, Azure OpenAI, OpenAI APIs, Anthropic Claude, Google Vertex AI, Azure AI Services, Model Context Protocol (MCP), Retrieval-Augmented Generation (RAG), prompt engineering, Responsible AI, AI governance, enterprise AI security"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_a0194fa4-29d"},"title":"Sr. Technical Architect","description":"<p>The Sr. Technical Architect is responsible for supporting Fortrea&#39;s technology vision, solution architecture strategy, and engineering architecture standards across the company&#39;s digital products, platforms, and technology portfolio.</p>\n<p>This role provides senior technical leadership by supporting cloud-native architecture patterns, AI-enabled architecture, engineering standards, integration strategies, platform engineering capabilities, reusable technology frameworks, and architecture governance that enable secure, scalable, resilient, high-performing, and AI-ready software solutions.</p>\n<p>As one of Fortrea&#39;s senior technical leaders, the Sr. Technical Architect partners closely with Product Management, Product Engineering, Platform Engineering, Data &amp; AI, Security, Infrastructure, and Enterprise Architecture to ensure technology investments align with business priorities while accelerating innovation and long-term platform evolution.</p>\n<p>The Sr. Technical Architect serves as a trusted technical advisor by driving modernization initiatives, enabling AI-powered software development, providing technical guidance to project teams and less-experienced colleagues, supporting engineering standards, and promoting engineering excellence across the Global Digital Foundry.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Support long-term solution architecture strategy, technology roadmaps, architecture principles, and technical standards across Fortrea&#39;s digital products and platforms.</li>\n<li>Support enterprise architecture standards, reusable design patterns, reference architectures, architecture decision records (ADRs), engineering guardrails, and governance processes that promote consistency, scalability, maintainability, and reuse.</li>\n<li>Support cloud-native architecture patterns utilizing Microsoft Azure, Kubernetes, containers, serverless computing, API-first design, event-driven architectures, distributed systems, and modern software engineering practices.</li>\n<li>Support solution architecture for digital products, SaaS platforms, APIs, integrations, mobile applications, cloud services, and shared engineering platforms.</li>\n<li>Define enterprise AI architecture patterns supporting Large Language Models (LLMs), Retrieval-Augmented Generation (RAG), AI agents, Model Context Protocol (MCP), vector databases, prompt orchestration, intelligent automation, and Responsible AI.</li>\n<li>Partner with Data &amp; AI teams to define reusable AI platform capabilities, enterprise AI governance, model integration strategies, and AI engineering standards.</li>\n<li>Drive architecture modernization initiatives including cloud migration, platform engineering, application modernization, technical debt reduction, API modernization, microservices adoption, and platform consolidation.</li>\n<li>Design reusable engineering platforms, shared services, Internal Developer Platforms (IDPs), developer enablement capabilities, and engineering accelerators that improve developer productivity.</li>\n<li>Define enterprise integration strategies including API Management, event streaming, messaging, asynchronous architectures, interoperability frameworks, FHIR/HL7 integration (where applicable), and secure service communication.</li>\n<li>Establish enterprise data architecture principles supporting Microsoft Fabric, cloud data platforms, analytics, data products, streaming architectures, governance, and enterprise data interoperability.</li>\n<li>Lead architecture reviews, technical assessments, proof-of-concepts, design workshops, technology evaluations, and solution design activities.</li>\n<li>Partner with Product Engineering leadership to ensure architecture aligns with customer needs, business priorities, product roadmaps, and engineering execution.</li>\n<li>Define architecture standards for security, Zero Trust, identity management, API security, secrets management, software supply chain security, privacy, compliance, resilience, observability, and operational excellence.</li>\n<li>Provide technical guidance to project teams and less-experienced colleagues by promoting software craftsmanship, engineering excellence, AI-assisted development, and architecture best practices.</li>\n<li>Build and lead Technical Architecture Communities of Practice that promote innovation, collaboration, reusable solutions, mentoring, technical standards, and continuous learning.</li>\n<li>Collaborate with Enterprise Architecture to align solution architecture with enterprise strategy, business capabilities, technology investments, and long-term transformation initiatives.</li>\n<li>Continuously evaluate emerging technologies including AI platforms, cloud services, engineering tools, developer productivity platforms, and software architecture trends that improve engineering effectiveness and customer outcomes.</li>\n<li>Establish architecture health metrics including technical debt reduction, architecture compliance, platform adoption, solution reuse, engineering productivity, operational reliability, and modernization progress.</li>\n<li>Identify architectural risks, technology constraints, operational dependencies, scalability challenges, and recommend mitigation strategies.</li>\n<li>Champion engineering excellence through reusable architecture, documentation standards, engineering best practices, software craftsmanship, and technical governance.</li>\n<li>Participate in technology strategy, architecture councils, engineering planning, executive technology discussions, and strategic investment decisions.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Computer Science, Software Engineering, Information Technology, Engineering, or related discipline. Equivalent experience will be considered.</li>\n<li>Deep expertise in enterprise software architecture, cloud-native application design, distributed systems, APIs, microservices, integration architecture, and modern software engineering practices.</li>\n<li>Strong knowledge of Microsoft Azure, Kubernetes, cloud-native platforms, containers, Infrastructure as Code, Platform Engineering, and modern application architecture.</li>\n<li>Strong understanding of Domain-Driven Design (DDD), Event-Driven Architecture, CQRS, Event Sourcing, Clean Architecture, Hexagonal Architecture, API-first design, and enterprise integration strategies.</li>\n<li>Strong understanding of AI platform architecture, intelligent automation, cloud-native AI services, and modern AI engineering principles.</li>\n<li>Expertise designing scalable, secure, resilient, observable, and highly available enterprise technology platforms.</li>\n<li>Strong knowledge of enterprise data architecture, cloud data services, data governance, integration platforms, and analytics ecosystems.</li>\n<li>Deep understanding of Zero Trust, identity management, secure software development lifecycle, privacy, software supply chain security, and regulatory compliance.</li>\n<li>Excellent communication, presentation, technical leadership, executive influence, and stakeholder management skills.</li>\n<li>Demonstrated ability to influence engineering organizations and executive leaders without direct management authority.</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>10+ years of progressive experience in Software Engineering, Solution Architecture, Technical Architecture, Platform Engineering, or related engineering disciplines.</li>\n<li>5+ years designing enterprise-scale SaaS platforms, digital products, APIs, cloud-native applications, distributed systems, and enterprise integrations.</li>\n<li>Demonstrated success supporting architecture strategies, technology roadmaps, engineering standards, and reusable architectural frameworks.</li>\n<li>Experience designing cloud-native platforms using Microsoft Azure, Kubernetes, Infrastructure as Code, containers, APIs, event-driven architectures, and microservices.</li>\n<li>Experience designing AI-enabled enterprise solutions using Azure OpenAI, OpenAI APIs, AI agents, Retrieval-Augmented Generation (RAG), intelligent automation, or machine learning services.</li>\n<li>Experience defining enterprise AI architecture, Responsible AI standards, AI governance, model integration strategies, and secure AI software development.</li>\n<li>Proven experience establishing API strategies, integration architectures, interoperability standards, messaging platforms, and enterprise integration patterns.</li>\n<li>Experience leading cloud transformation, application modernization, platform engineering, technical debt reduction, and enterprise modernization initiatives.</li>\n<li>Experience partnering with Product Management, Product Engineering, Platform Engineering, Data &amp; AI, Security, Infrastructure, Enterprise Architecture, and executive leadership.</li>\n<li>Experience conducting architecture reviews, technical governance, design reviews, proof-of-concepts, technical assessments, and technology evaluations.</li>\n<li>Demonstrated success balancing customer needs, business priorities, operational requirements, technical constraints, and long-term technology strategy.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Technical-Architect_265717","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Technical-Architect_265717","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Microsoft Azure","Kubernetes","cloud-native application design","distributed systems","APIs","microservices","integration architecture","modern software engineering practices","Domain-Driven Design (DDD)","Event-Driven Architecture","CQRS","Event Sourcing","Clean Architecture","Hexagonal Architecture","API-first design","enterprise integration strategies","AI platform architecture","intelligent automation","cloud-native AI services","modern AI engineering principles","Zero Trust","identity management","secure software development lifecycle","privacy","software supply chain security","regulatory compliance"],"x-skills-preferred":["Azure OpenAI","OpenAI APIs","Anthropic Claude","Google Vertex AI","Large Language Models (LLMs)","Retrieval-Augmented Generation (RAG)","AI agents","Model Context Protocol (MCP)","vector databases","Azure Kubernetes Service (AKS)","Azure API Management","Microsoft Fabric","Azure Landing Zones","Azure DevOps","GitHub Enterprise","GitHub Actions","Terraform","Bicep","Docker","Helm","Infrastructure as Code"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Microsoft Azure, Kubernetes, cloud-native application design, distributed systems, APIs, microservices, integration architecture, modern software engineering practices, Domain-Driven Design (DDD), Event-Driven Architecture, CQRS, Event Sourcing, Clean Architecture, Hexagonal Architecture, API-first design, enterprise integration strategies, AI platform architecture, intelligent automation, cloud-native AI services, modern AI engineering principles, Zero Trust, identity management, secure software development lifecycle, privacy, software supply chain security, regulatory compliance, Azure OpenAI, OpenAI APIs, Anthropic Claude, Google Vertex AI, Large Language Models (LLMs), Retrieval-Augmented Generation (RAG), AI agents, Model Context Protocol (MCP), vector databases, Azure Kubernetes Service (AKS), Azure API Management, Microsoft Fabric, Azure Landing Zones, Azure DevOps, GitHub Enterprise, GitHub Actions, Terraform, Bicep, Docker, Helm, Infrastructure as Code"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_4e72c766-9a9"},"title":"Director, Mobile Application Engineering","description":"<p>The Director, Mobile Application Engineering is responsible for supporting and executing Fortrea&#39;s mobile engineering strategy in alignment with established enterprise standards while transforming how mobile products are designed, developed, tested, secured, and delivered.</p>\n<p>This leader will build and lead high-performing global engineering teams responsible for delivering secure, scalable, high-performing mobile applications that enhance customer, employee, and patient experiences. The role combines technical leadership, organizational development, product engineering, and innovation to accelerate Fortrea&#39;s digital transformation.</p>\n<p>The Director will drive adoption of AI-assisted software engineering, cloud-native architectures, DevSecOps, automation, platform engineering, and modern mobile development practices to improve engineering productivity, software quality, and speed of delivery.</p>\n<p>Working closely with Product Management, Architecture, Security, Infrastructure, Data &amp; AI, and Business stakeholders, this leader will translate strategic business objectives into technical execution while fostering a culture of engineering excellence, continuous improvement, innovation, and accountability.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Support and execute the mobile engineering strategy aligned with established Fortrea product and business objectives.</li>\n<li>Build, lead, mentor, and develop high-performing engineering managers, architects, technical leads, and software engineers while creating strong succession plans and career development opportunities.</li>\n<li>Lead the design, architecture, development, testing, deployment, and lifecycle management of enterprise mobile applications across iOS, Android, and modern cross-platform technologies.</li>\n<li>Manage mobile architecture standards, reusable platforms, shared SDKs, engineering frameworks, and governance based on already established enterprise standards that enable rapid product delivery across multiple applications.</li>\n<li>Drive adoption of AI-assisted software engineering tools and intelligent development practices to improve developer productivity, software quality, automated testing, documentation, code generation, and release velocity.</li>\n<li>Partner with Product Management to build customer-centric digital products that continuously evolve through customer feedback, analytics, experimentation, and data-driven decision making.</li>\n<li>Evaluate and implement Generative AI capabilities within mobile applications to improve customer, employee, and patient experiences.</li>\n<li>Champion engineering excellence through Agile, DevSecOps, CI/CD, Infrastructure as Code, automated quality engineering, and modern software delivery practices.</li>\n<li>Improve developer experience through automation, self-service engineering platforms, modern development environments, developer tooling, and engineering productivity initiatives.</li>\n<li>Ensure solutions are secure, scalable, resilient, performant, observable, maintainable, and aligned with enterprise architecture and cybersecurity standards.</li>\n<li>Partner with Security, Privacy, Compliance, and Risk organizations to ensure mobile applications meet regulatory, HIPAA, privacy, security, and secure software development lifecycle requirements.</li>\n<li>Collaborate with executive leadership to define technology strategy, investment priorities, engineering roadmaps, and long-term platform evolution.</li>\n<li>Drive operational excellence through observability, telemetry, monitoring, crash analytics, feature flags, experimentation, and performance optimization.</li>\n<li>Manage engineering metrics including DORA metrics, application health, engineering productivity, operational reliability, software quality, customer adoption, and business outcomes.</li>\n<li>Lead technical risk management, production support, incident response, disaster recovery, and continuous service improvement activities.</li>\n<li>Evaluate emerging mobile technologies, AI platforms, engineering tools, frameworks, and industry trends that improve innovation and accelerate software delivery.</li>\n<li>Manage engineering budgets, vendor relationships, resource planning, strategic investments, and technology partnerships.</li>\n<li>Foster a high-performance engineering culture centered on ownership, collaboration, innovation, technical excellence, continuous learning, diversity, inclusion, accountability, and customer focus.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree in computer science, Software Engineering, Information Technology, or related discipline. Equivalent experience will be considered.</li>\n<li>Strong understanding of modern software engineering principles, architecture patterns, cloud-native application development, and enterprise mobile engineering.</li>\n<li>Expertise in native mobile development, cross-platform frameworks, API-first architecture, distributed systems, and cloud-connected mobile solutions.</li>\n<li>Strong knowledge of secure software development lifecycle, mobile application security, privacy, authentication, identity management, and modern cybersecurity practices.</li>\n<li>Demonstrated experience implementing engineering governance, architecture standards, and engineering excellence initiatives.</li>\n<li>Strong executive communication, organizational leadership, stakeholder management, and strategic planning skills.</li>\n<li>Proven ability to influence technical and business decisions across executive leadership and cross-functional organizations.</li>\n<li>Demonstrated success leading large-scale enterprise technology transformations within globally distributed engineering organizations.</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>10+ years of progressive software engineering experience, including significant experience delivering enterprise mobile applications and digital products.</li>\n<li>5+ years leading engineering managers, architects, or globally distributed software engineering organizations.</li>\n<li>Demonstrated experience supporting and executing mobile engineering strategies based on already established enterprise standards.</li>\n<li>Proven success leading development and delivery of enterprise-scale iOS, Android, React Native, Flutter, Kotlin Multiplatform, or equivalent mobile platforms.</li>\n<li>Experience building reusable engineering platforms, shared services, developer tooling, and engineering frameworks.</li>\n<li>Experience implementing AI-assisted software development practices and evaluating emerging AI technologies that improve engineering productivity.</li>\n<li>Experience implementing DevSecOps, CI/CD pipelines, Infrastructure as Code, automated testing, quality engineering, and modern software delivery practices.</li>\n<li>Experience improving engineering organizations using data-driven metrics including DORA Metrics, operational KPIs, engineering productivity, and software quality indicators.</li>\n<li>Experience managing multiple engineering roadmaps, budgets, strategic investments, vendors, and resource planning.</li>\n<li>Demonstrated success partnering with Product Management, Architecture, Data &amp; AI, Security, Infrastructure, and executive leadership to deliver enterprise technology solutions.</li>\n<li>Experience leading geographically distributed engineering organizations across multiple regions and cultures.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Work is performed in an office environment with exposure to electrical office equipment.</li>\n<li>Occasional drives to site locations with occasional travel both domestic and international.</li>\n</ul>\n<p><strong>Physical Requirements:</strong></p>\n<ul>\n<li>Frequently stationary for 6-8 hours per day.</li>\n<li>Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.</li>\n<li>Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.</li>\n<li>Ability to access and use a variety of computer software developed both in-house and off-the-shelf.</li>\n<li>Light to moderate lifting and carrying, or moving of objects, including luggage and laptop computer with a maximum lift of 15-20 lbs.</li>\n<li>Regular and consistent attendance.</li>\n<li>Varied hours may be required.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Director--Mobile-Application-Engineering_265718-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Director--Mobile-Application-Engineering_265718-1","x-work-arrangement":"hybrid","x-experience-level":"executive","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["modern software engineering principles","cloud-native application development","enterprise mobile engineering","native mobile development","cross-platform frameworks","API-first architecture","distributed systems","cloud-connected mobile solutions","secure software development lifecycle","mobile application security","privacy","authentication","identity management","cybersecurity practices","engineering governance","architecture standards","engineering excellence initiatives"],"x-skills-preferred":["AI-assisted software engineering","Large Language Models (LLMs)","Retrieval-Augmented Generation (RAG)","conversational AI","intelligent search","recommendation engines","AI agents","Azure OpenAI","OpenAI APIs","Anthropic","Google Vertex AI","Azure AI Services","cloud-native architectures","Microsoft Azure","AWS","Google Cloud Platform","Kubernetes","containers","microservices","event-driven architecture","API Management","Azure Functions","serverless computing","modern observability platforms","Datadog","New Relic","Sentry","Crashlytics","Azure Monitor"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"modern software engineering principles, cloud-native application development, enterprise mobile engineering, native mobile development, cross-platform frameworks, API-first architecture, distributed systems, cloud-connected mobile solutions, secure software development lifecycle, mobile application security, privacy, authentication, identity management, cybersecurity practices, engineering governance, architecture standards, engineering excellence initiatives, AI-assisted software engineering, Large Language Models (LLMs), Retrieval-Augmented Generation (RAG), conversational AI, intelligent search, recommendation engines, AI agents, Azure OpenAI, OpenAI APIs, Anthropic, Google Vertex AI, Azure AI Services, cloud-native architectures, Microsoft Azure, AWS, Google Cloud Platform, Kubernetes, containers, microservices, event-driven architecture, API Management, Azure Functions, serverless computing, modern observability platforms, Datadog, New Relic, Sentry, Crashlytics, Azure Monitor"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bb68b81c-3ad"},"title":"Manager, Engineering Excellence & Quality Engineering","description":"<p>The Manager, Engineering Excellence &amp; Quality Engineering is responsible for supporting and executing Fortrea&#39;s Engineering Excellence and Quality Engineering practices across the Global Digital Foundry organization.</p>\n<p>This leader drives engineering maturity by supporting standards, AI-enabled quality engineering practices, software craftsmanship, test automation, engineering governance, performance engineering, developer productivity, and continuous improvement initiatives that improve software quality, delivery effectiveness, and customer outcomes.</p>\n<p>Working closely with Product Engineering, Architecture, Platform Engineering, DevOps, Security, Data &amp; AI, and Product Management, this role champions modern engineering practices that enable teams to build secure, scalable, reliable, and high-quality software.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Support and execute Fortrea&#39;s Engineering Excellence and Quality Engineering strategy, roadmap, standards, governance model, and operating framework.</li>\n<li>Build, lead, mentor, and develop high-performing Quality Engineering professionals while fostering technical growth, leadership development, succession planning, and continuous learning.</li>\n<li>Support enterprise engineering excellence standards including software craftsmanship, coding standards, architecture reviews, pull request quality, secure coding practices, technical debt management, release readiness, and engineering governance.</li>\n<li>Champion Shift Left Engineering by embedding quality, security, accessibility, performance, reliability, and compliance practices throughout the software development lifecycle.</li>\n<li>Drive adoption of AI-assisted Quality Engineering practices including intelligent test generation, autonomous testing, automated test maintenance, defect prediction, release risk analysis, AI-assisted code reviews, and engineering automation.</li>\n<li>Evaluate emerging AI technologies that improve engineering productivity, software quality, release confidence, developer experience, and customer satisfaction.</li>\n<li>Support enterprise standards for Responsible AI testing, validation, governance, and quality assurance for AI-enabled products and intelligent software solutions.</li>\n<li>Support testing practices across unit, integration, API, contract, UI, end-to-end, performance, resilience, security, accessibility, regression, and user acceptance testing.</li>\n<li>Partner with Platform Engineering and DevOps teams to embed automated quality gates, testing frameworks, compliance validation, security controls, and Quality as Code practices into CI/CD pipelines.</li>\n<li>Support quality, reliability, performance, observability, and production readiness practices that improve software delivery outcomes.</li>\n<li>Use engineering metrics, quality indicators, defect trends, test coverage, release quality, and operational performance data to identify improvement opportunities.</li>\n<li>Perform quality benchmarking, root cause analysis, trend analysis, defect prevention, engineering maturity assessments, and continuous improvement initiatives.</li>\n<li>Provide guidance to engineering teams and technical leaders on software craftsmanship, engineering excellence, testing strategy, AI-assisted engineering, and modern software development practices.</li>\n<li>Support engineering Communities of Practice (CoPs) that promote technical standards, knowledge sharing, innovation, mentoring, and continuous improvement.</li>\n<li>Partner with Product Engineering, Architecture, Platform Engineering, DevOps, Security, Infrastructure, and Product Management to improve engineering maturity.</li>\n<li>Support software validation and regulatory compliance activities for highly regulated healthcare and life sciences solutions.</li>\n<li>Continuously evaluate emerging engineering tools, AI platforms, automation technologies, testing frameworks, and software engineering practices that improve software delivery and engineering effectiveness.</li>\n<li>Support team capacity planning, resource planning, tooling needs, vendor coordination, and quality improvement initiatives.</li>\n<li>Foster a culture centered on ownership, software craftsmanship, quality, innovation, collaboration, accountability, continuous learning, and engineering excellence.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Computer Science, Software Engineering, Information Technology, or related discipline. Equivalent experience will be considered.</li>\n<li>Strong understanding of modern software engineering, Agile delivery, Engineering Excellence, DevOps, CI/CD, Platform Engineering, and Quality Engineering principles.</li>\n<li>Deep knowledge of enterprise test automation, software quality practices, engineering governance, software craftsmanship, and engineering maturity frameworks.</li>\n<li>Experience with automated testing, Quality as Code, engineering automation, Shift Left Engineering, and modern software delivery methodologies.</li>\n<li>Strong understanding of cloud-native architectures, distributed systems, performance engineering, observability, resilience engineering, and operational excellence.</li>\n<li>Strong leadership, communication, facilitation, stakeholder management, organizational development, and influencing skills.</li>\n<li>Demonstrated ability to influence engineering organizations and technical leaders without direct authority.</li>\n<li>Strong analytical and data-driven decision-making skills focused on continuous improvement and engineering effectiveness.</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>8+ years of progressive experience in Software Engineering, Quality Engineering, DevOps, Platform Engineering, Software Architecture, or related engineering disciplines.</li>\n<li>3+ years leading Quality Engineering teams, Engineering Excellence programs, or engineering improvement initiatives.</li>\n<li>Demonstrated experience supporting Quality Engineering strategies, Engineering Excellence programs, or engineering improvement practices.</li>\n<li>Proven success implementing test automation across multiple products, platforms, or engineering teams.</li>\n<li>Experience implementing AI-assisted software engineering and intelligent testing capabilities that improve engineering productivity and software quality.</li>\n<li>Experience supporting engineering standards, governance processes, software craftsmanship practices, release readiness criteria, and engineering maturity models.</li>\n<li>Experience implementing DORA Metrics, engineering productivity scorecards, software quality KPIs, and continuous improvement programs.</li>\n<li>Experience supporting performance engineering, resilience testing, production quality monitoring, and operational excellence initiatives.</li>\n<li>Experience partnering with Product Engineering, Platform Engineering, DevOps, Architecture, Security, and Data &amp; AI teams.</li>\n<li>Experience supporting software validation, regulatory compliance, or highly regulated software environments.</li>\n<li>Demonstrated success supporting improvement initiatives focused on Engineering Excellence, Quality Engineering, or software delivery modernization.</li>\n<li>Strong experience utilizing engineering metrics, operational analytics, and quality data to improve engineering effectiveness and business outcomes.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Work is performed in an office environment with exposure to electrical office equipment.</li>\n<li>Occasional drives to site locations with occasional travel both domestic and international.</li>\n</ul>\n<p><strong>Physical Requirements:</strong></p>\n<ul>\n<li>Frequently stationary for 6-8 hours per day.</li>\n<li>Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.</li>\n<li>Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.</li>\n<li>Ability to access and use a variety of computer software developed both in-house and off-the-shelf.</li>\n<li>Light to moderate lifting and carrying, or moving of objects, including luggage and laptop computer with a maximum lift of 15-20 lbs.</li>\n<li>Regular and consistent attendance.</li>\n<li>Varied hours may be required.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Manager--Engineering-Excellence---Quality-Engineering_265715","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Manager--Engineering-Excellence---Quality-Engineering_265715","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Software Engineering","Quality Engineering","DevOps","Platform Engineering","Agile delivery","Engineering Excellence","CI/CD","Test Automation","AI-assisted software engineering","Shift Left Engineering"],"x-skills-preferred":["AI-powered Quality Engineering","Intelligent test generation","Autonomous testing","Automated test maintenance","Defect prediction","Release risk analysis","AI-assisted code reviews","Engineering copilots","Responsible AI principles","Prompt engineering","AI governance","Model evaluation","AI quality assurance","AI security"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Software Engineering, Quality Engineering, DevOps, Platform Engineering, Agile delivery, Engineering Excellence, CI/CD, Test Automation, AI-assisted software engineering, Shift Left Engineering, AI-powered Quality Engineering, Intelligent test generation, Autonomous testing, Automated test maintenance, Defect prediction, Release risk analysis, AI-assisted code reviews, Engineering copilots, Responsible AI principles, Prompt engineering, AI governance, Model evaluation, AI quality assurance, AI security"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_25cd8dcb-47a"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conduct site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Prepare and implement project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguard data integrity by careful source document review, source document verification, query generation, and resolution</li>\n<li>Confirm Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current</li>\n<li>Guarantee that the study Investigational Product inventory and accountability is accurate</li>\n<li>Ensure adherence to global quality control and CRA performance metrics</li>\n<li>Ensure audit readiness at site level</li>\n<li>Act as a Lead CRA as assigned</li>\n</ul>\n<p><strong>General On-Site Monitoring Responsibilities:</strong></p>\n<ul>\n<li>Ensure study staff have received proper materials and instructions to safely enter subjects into the study</li>\n<li>Perform eligibility review and verify screening, informed consent procedures, and protocol requirements</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance</li>\n<li>Identify deficiencies, deviations, and discrepancies, and initiate corrective action</li>\n<li>Perform monitoring tasks efficiently and manage travel expenses economically</li>\n<li>Travel to study sites, prepare and submit trip reports, and perform eCRF review and source data verification</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession</li>\n<li>Thorough understanding of ICH GCP Guidelines and local regulatory requirements</li>\n<li>Basic understanding of the clinical trial process</li>\n<li>Fluent in local office language and in English</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>Minimum 2 years of Clinical Monitoring experience</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines</li>\n<li>Ability to work with minimal supervision</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>Additional years of experience in a related field</li>\n<li>Phase I monitoring experience</li>\n<li>Life Science or Nursing qualification</li>\n<li>Specific skills, systems, certifications, and/or licenses</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Must be able to sit at a computer for long periods</li>\n<li>Must be able to use hands to finger, handle or touch objects, tools or controls</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours</li>\n<li>Travel Requirement is 60% of the time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Kuala-Lumpur/Clinical-Research-Associate-2_265638","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Kuala-Lumpur/Clinical-Research-Associate-2_265638","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Clinical Monitoring","Source Document Review","Data Integrity","Regulatory Compliance"],"x-skills-preferred":["Fortrea SOPs","Phase I monitoring","Life Science or Nursing qualification","e-clinical systems"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-30T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kuala Lumpur"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, Clinical Monitoring, Source Document Review, Data Integrity, Regulatory Compliance, Fortrea SOPs, Phase I monitoring, Life Science or Nursing qualification, e-clinical systems"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c89d2664-a0d"},"title":"Clinical Trial Manager II","description":"<p>The Clinical Trial Manager II owns the clinical delivery and operational oversight of clinical research trials within the core project team.</p>\n<p>The CTM II collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.</p>\n<p>While the role may occasionally support larger, more complex trials under the guidance of a Senior Clinical Trial Manager, it is generally expected to manage most studies independently and comprehensively.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>End-to-end oversight of start-up and clinical responsibilities,from site identification through to database lock,through proactive management of project scope, timelines, milestones, and budget.</li>\n<li>Ensure start-up and clinical project plans address identified risks while adhering to professional standards, SOPs, client, and regulatory requirements.</li>\n<li>Proactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems.</li>\n<li>Responsible for financial aspects of clinical and start-up activities, including revenue forecasting, adherence to contracted scope, and oversight of scope modifications.</li>\n<li>Ensure project team awareness and tracking of Key Project Indicators (KPI) for any client-specific start-up and clinical metrics.</li>\n<li>Ensure and plans for start-up and clinical resources with accurate projections for the resourcing teams.</li>\n<li>Develop and implement the site activation and recruitment strategy in collaboration with project teams.</li>\n<li>Lead and oversee site identification and site selection.</li>\n<li>Oversight of Informed Consent Form development and translations.</li>\n<li>Oversight of essential document creation and collection, including insurance.</li>\n<li>Oversight of the development, negotiation, and execution of Clinical Trial Agreements (CTA), including site budgets.</li>\n<li>Lead the end-to-end process of regulatory/ethics committee submissions, approvals, and tracking.</li>\n<li>Ensure clinical and ancillary supplies -including import/export logistics and supply destruction processes- are in place as applicable.</li>\n<li>Manage operational aspects to support subject recruitment and retention, patient safety, vendor performance, and the monitoring visit strategy.</li>\n<li>Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint protection.</li>\n<li>Ensure inspection-readiness through quality oversight of TMF, monitoring reports, protocol deviations and issue management.</li>\n<li>Oversight and approval of site payments, including payment reconciliation.</li>\n<li>Foster effective communication and collaboration with clients and cross-functional project teams in a global and multicultural environment.</li>\n<li>Ability to lead client-facing calls to communicate project status updates and demonstrate operational control of start-up and clinical deliverables.</li>\n<li>Support new business with active participation in pre-award preparation as required.</li>\n<li>Provides training and support to new and/or junior team members</li>\n<li>All other duties as needed or assigned.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.</li>\n<li>Fluent in English, both written and verbal</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Five or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.</li>\n<li>Comprehensive knowledge of GCP, ICH, and regulatory guidelines.</li>\n<li>Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).</li>\n<li>Effective leadership in remote and global environment.</li>\n<li>Strong communication, planning, and organizational abilities.</li>\n<li>Proven team motivational skills.</li>\n<li>Proficiency in balancing concurrent tasks within time-sensitive environments.</li>\n<li>Financial awareness and use of tracking systems/tools.</li>\n<li>Demonstrated independent problem-solving and risk management mindset.</li>\n<li>Demonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.</li>\n</ul>\n<p><strong>Preferred Qualifications Include:</strong></p>\n<ul>\n<li>Master’s or other advanced degree.</li>\n<li>PMP certification or equivalent.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location.</li>\n<li>Travel requirements: up to 20% (global – primarily domestic and international)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/Clinical-Trial-Manager-III_265687","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/Clinical-Trial-Manager-III_265687","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["GCP","ICH","regulatory guidelines","Microsoft Office","EDC","CTMS","eTMF","Veeva Vault","Medidata","English"],"x-skills-preferred":["Master’s degree","PMP certification"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-09-30T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Seoul"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"GCP, ICH, regulatory guidelines, Microsoft Office, EDC, CTMS, eTMF, Veeva Vault, Medidata, English, Master’s degree, PMP certification"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_5fa08828-81d"},"title":"Clinical Research Associate (CRA)","description":"<p>We are seeking a Clinical Research Associate (CRA) to join our team. As a CRA, you will have site management responsibility for clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, and applicable project plans and Sponsor requirements.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conduct site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Prepare and implement project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements</li>\n<li>Safeguard data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines</li>\n<li>Confirm Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial</li>\n<li>Guarantee that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements</li>\n<li>Ensure adherence to global quality control and CRA performance metrics</li>\n<li>Ensure audit readiness at site level</li>\n<li>Act in the project role of a Lead CRA as assigned</li>\n</ul>\n<p><strong>General On-Site Monitoring Responsibilities:</strong></p>\n<ul>\n<li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study</li>\n<li>Perform eligibility review, verify screening, informed consent procedures, and protocol requirements are adhered to according to applicable regulatory requirements</li>\n<li>Ensure the integrity of the source data reported by careful source document review</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance</li>\n<li>Identify deficiencies, deviations, and discrepancies, and initiate corrective action as required</li>\n<li>Perform required monitoring tasks in an efficient manner, according to SOPs and established guidelines</li>\n<li>Travel, including air travel, may be required and is an essential function of the job</li>\n<li>Prepare and submit accurate and timely trip reports</li>\n<li>Independently perform eCRF review, 100% source data verification, query generation, and resolution against established data review guidelines</li>\n<li>Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation, and site management</li>\n<li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems</li>\n<li>Track IP shipments and supplies, as needed</li>\n<li>Track and follow-up on serious adverse events as assigned</li>\n<li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met</li>\n<li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned</li>\n<li>Attend investigators&#39; meetings, project team meetings, and teleconferences, and others as needed</li>\n<li>Present training content for site initiation</li>\n<li>Assist with training of new employees</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Minimum 2 years of site monitoring experience</li>\n<li>Oncology experience is required</li>\n<li>Experience in Start-up, site maintenance, and Close-outs</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Manila/Clinical-Research-Associate--Pooling-for-future-openings-_265731","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Manila/Clinical-Research-Associate--Pooling-for-future-openings-_265731","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Fortrea's Standard Operating Procedures","clinical trial management","site monitoring","data integrity","regulatory 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responsibilities include:</p>\n<ul>\n<li>Conducting site monitoring, including routine monitoring and closeout of clinical sites</li>\n<li>Maintaining study files and conducting pre-study and initiation visits</li>\n<li>Liaising with vendors and performing other duties as assigned</li>\n<li>Ensuring study staff have received proper materials and instructions to safely enter patients into the study</li>\n<li>Verifying informed consent procedures and protocol requirements are adhered to</li>\n<li>Reviewing data for missing or implausible entries</li>\n<li>Managing travel expenses efficiently</li>\n<li>Preparing accurate and timely trip reports</li>\n<li>Serving as lead monitor for a protocol or project</li>\n<li>Participating in protocol development and clinical trial report writing</li>\n<li>Interacting with internal work groups to evaluate needs, resources, and timelines</li>\n</ul>\n<p>The Senior CRA will also be responsible for:</p>\n<ul>\n<li>Registry management</li>\n<li>Feasibility work</li>\n<li>Quality Control visits</li>\n<li>Recruitment of investigators</li>\n<li>Budget negotiations</li>\n<li>Serious Adverse Event reporting</li>\n<li>CRF review and query generation</li>\n<li>Training and mentoring new employees</li>\n</ul>\n<p>Requirements include:</p>\n<ul>\n<li>University or college degree in life sciences or related field</li>\n<li>Certification in a related allied health profession or nursing certification</li>\n<li>Thorough knowledge of regulatory requirements</li>\n<li>Understanding of the drug development process</li>\n<li>Fluent in local office language and English</li>\n<li>High competence level of Clinical Monitoring experience</li>\n<li>Advanced study site management skills</li>\n<li>Ability to work with minimal supervision</li>\n<li>Good planning and organisation skills</li>\n<li>Valid Driver&#39;s License</li>\n</ul>\n<p>Travel requirements: 60-80% overnight.</p>\n<p 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licence"],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-01T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Melbourne"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Monitoring, Site Management, Regulatory Guidelines, Protocol Development, Clinical Trial Report Writing, CRF Review"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bfa3847a-6c9"},"title":"Senior Clinical Research Associate II (SCRA II)","description":"<p>Fortrea&#39;s FSP department in Paris is recruiting a Senior Clinical Research Associate II (SCRA II).</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Monitor clinical trials by conducting site visits to ensure compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP), with 40% of site visits in France.</li>\n<li>Manage sites by serving as the primary point of contact for investigational sites, ensuring smooth study operations.</li>\n<li>Perform Source Document Verification (SDV) by reviewing and verifying the accuracy of clinical data collected from study sites.</li>\n<li>Provide investigator training and support by offering ongoing training to site staff on study protocols and regulatory requirements.</li>\n<li>Prepare monitoring reports, maintain study records, and contribute to overall trial documentation.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Life sciences university degree or certification in a related allied health profession from an accredited institution (e.g., nursing licensure).</li>\n<li>Thorough understanding of ICH GCP Guidelines and local regulatory requirements.</li>\n<li>Knowledge of monitoring procedures and a basic understanding of the clinical trial process.</li>\n<li>Fluency in English, both written and verbal.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Office-based or remote position.</li>\n<li>Career growth opportunities in a supportive environment.</li>\n<li>Dedicated line manager.</li>\n<li>Opportunity to work directly with a leading sponsor on innovative studies.</li>\n<li>Attractive salary and Fortrea benefits.</li>\n</ul>\n<p>If you&#39;re passionate about clinical research, enjoy collaborative environments, and seek exciting career growth, we&#39;d love to hear from you!</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Paris/Senior-CRA-II---Sponsor-dedicated_265405-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Paris/Senior-CRA-II---Sponsor-dedicated_265405-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":null,"x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Good Clinical Practice","clinical trial management","regulatory 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As a Site Budget &amp; Contract Specialist, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support clinical research efforts.</p>\n<p>In this role, you will be part of the FSPx team and work directly with a renowned key sponsor to advance the development of innovative, life-changing medications.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials.</li>\n<li>Ensure compliance with SOPs, regulatory guidelines, and contractual obligations.</li>\n<li>Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution.</li>\n<li>Identify and escalate contractual issues to management as needed.</li>\n<li>Support the internal review, revision, and approval process of contracts before forwarding them to external parties.</li>\n<li>Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution.</li>\n<li>Maintain electronic and paper contract files, ensuring accuracy and accessibility.</li>\n<li>Assist in the continuous improvement of departmental processes and procedures.</li>\n<li>Provide regular status updates to management and study teams.</li>\n</ul>\n<p><strong>Required Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable (UK/EU).</li>\n<li>Equivalent relevant experience may be considered in lieu of educational requirements.</li>\n<li>2–4 years of experience in contract negotiation, clinical research, or a related field.</li>\n<li>Strong understanding of ICH GCP guidelines and clinical research processes.</li>\n<li>Excellent negotiation, communication, and organisational skills.</li>\n<li>Ability to work independently and manage multiple priorities in a fast-paced environment.</li>\n<li>Proficiency in Microsoft Office and contract tracking systems.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive salary and performance-based incentives.</li>\n<li>Flexible work arrangements (remote/hybrid options).</li>\n<li>Professional growth opportunities in a collaborative and innovative environment.</li>\n<li>The opportunity to work on cutting-edge clinical research projects.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Site-Budget---Contract-Specialist_251029","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Site-Budget---Contract-Specialist_251029","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP guidelines","contract negotiation","clinical research","Microsoft Office"],"x-skills-preferred":["university-level law degree","contract tracking systems"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-01T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Maidenhead"}},"employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"ICH GCP guidelines, contract negotiation, clinical research, Microsoft Office, university-level law degree, contract tracking systems"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_debc844e-ac4"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to join our team. 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meetings, project team meetings, and teleconferences, and others as needed</li>\n<li>Present training content for site initiation</li>\n<li>Assist with training of new employees</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements</li>\n<li>Thorough knowledge of monitoring procedures</li>\n<li>Basic understanding of the clinical trial process</li>\n<li>Fluent in local office language and in English, both written and verbal</li>\n<li>Relevant and equivalent experience in lieu of educational requirements may be considered</li>\n</ul>\n<p>Experience:</p>\n<ul>\n<li>A minimum of 2 years of Clinical Monitoring experience</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines</li>\n<li>Ability to work with minimal supervision</li>\n<li>Understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives, and follow-up of SAEs</li>\n<li>Good planning, organization, and problem-solving abilities</li>\n<li>Works efficiently and effectively in a matrix environment</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>One or more additional years of experience in a related field</li>\n<li>Phase I monitoring experience</li>\n<li>Life Science or Nursing qualification</li>\n<li>Specific skills, systems, certifications, and/or licenses preferred</li>\n<li>Personal characteristics such as leadership, problem-solving, and interpersonal skills</li>\n<li>Good attention to detail, methodical approach to work, and good understanding of medical and clinical research terminology and clinical research processes</li>\n</ul>\n<p>Physical Demands/Work Environment:</p>\n<ul>\n<li>Must be able to sit at a computer for long periods of time</li>\n<li>Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment (administrative only)</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours as required by the role</li>\n<li>Travel Requirement is 60% of the time (traveling to study sites)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Buenos-Aires/CRA-II---Sr-CRA_263925","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Buenos-Aires/CRA-II---Sr-CRA_263925","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","clinical trial monitoring","site management","data integrity","regulatory compliance"],"x-skills-preferred":["Fortrea SOPs","Phase I monitoring","Life Science or Nursing qualification","e-clinical systems","clinical trial management system (CTMS)"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-01T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Buenos Aires"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, clinical trial monitoring, site management, data integrity, regulatory compliance, Fortrea SOPs, Phase I monitoring, Life Science or Nursing qualification, e-clinical systems, clinical trial management system (CTMS)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_87a39e6e-b77"},"title":"Associate Clinical Data Manager – sponsor-dedicated - remote","description":"<p>Join Fortrea&#39;s Clinical Data Management sponsor-dedicated team as an Associate Clinical Data Manager, working remotely. You&#39;ll be part of a world-leading team, working in a collaborative environment with exceptional people.</p>\n<p>The Associate Clinical Data Manager role involves managing the full cycle of Clinical Data Management queries, working closely with Senior CDMs, Data Coordinators, Statistical Programmers, and others.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Assist and lead operations teams, developing project documentation, system setup, data validation processes, and procedures.</li>\n<li>Build study milestone timelines and ensure on-time deliverables.</li>\n<li>Lead internal and external DM meetings.</li>\n<li>Proactively manage risks and resolve issues related to Clinical Data Management.</li>\n<li>Develop an understanding of CDASH and SDTM standards and their impact on programming teams.</li>\n<li>Conduct lessons learned and disseminate across the organization.</li>\n<li>Act as a team leader or mentor for Clinical Data Management colleagues.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>University/college degree in life sciences, pharmacy, or a related subject.</li>\n<li>Experience in clinical data management as a Lead DM or Senior CDA.</li>\n<li>Excellent communication and presentation skills.</li>\n<li>In-depth knowledge of clinical trial processes, data management, and biometrics.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive compensation packages, including pension contributions and health insurance plans.</li>\n<li>Flexible working hours and remote work arrangements.</li>\n<li>Thorough onboarding and personalized development planning.</li>\n<li>Permanent employment contract with Fortrea Drug Development.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bucharest/Associate-Clinical-Data-Manager---FSP_265782","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bucharest/Associate-Clinical-Data-Manager---FSP_265782","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical data management","CDASH","SDTM","biometrics"],"x-skills-preferred":["life sciences","pharmacy"],"x-benefits":["pension","health_insurance"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-02T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bucharest"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical data management, CDASH, SDTM, biometrics, life sciences, pharmacy"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_825a0a4d-053"},"title":"Senior Director, Technology Engineering & Site Lead","description":"<p>The Senior Director, Technology Engineering &amp; Site Lead serves as the senior engineering leader for Fortrea&#39;s engineering organisation, the primary Foundry leadership representative for the site, and a strategic partner to the Head of the Global Digital Foundry.</p>\n<p>This role is responsible for providing strategic and operational leadership across engineering teams, driving delivery excellence, organisational effectiveness, workforce strategy, technology execution, and engineering innovation aligned to enterprise priorities.</p>\n<p>The incumbent partners closely with Product, Technology, Architecture, Data &amp; AI, and business leaders to ensure the successful delivery of scalable, reliable, secure, and compliant technology solutions.</p>\n<p><strong>Strategic Leadership</strong></p>\n<ul>\n<li>Lead multiple engineering organisations within the Global Digital Foundry, ensuring alignment with enterprise technology and Foundry priorities.</li>\n<li>Translate business and technology objectives into actionable engineering strategies and delivery plans.</li>\n<li>Partner with senior Technology, Product, and business leaders to drive execution of critical initiatives and organisational goals.</li>\n<li>Contribute to long-term technology and workforce planning efforts that support organisational growth and scalability.</li>\n<li>Serve as the senior Foundry leader for the hub site, representing engineering interests in global leadership forums.</li>\n</ul>\n<p><strong>Engineering Delivery &amp; Operational Excellence</strong></p>\n<ul>\n<li>Lead engineering teams responsible for delivering scalable, reliable, and secure technology solutions that support business objectives.</li>\n<li>Lead the adoption and implementation of AI-assisted software engineering practices across the organisation.</li>\n<li>Partner with Product, Data &amp; AI, and Architecture teams to identify, prioritise, and operationalise AI capabilities that accelerate software delivery.</li>\n<li>Ensure the successful execution of engineering initiatives through effective governance, prioritisation, resource allocation, and performance management.</li>\n</ul>\n<p><strong>People Leadership &amp; Talent Development</strong></p>\n<ul>\n<li>Lead, develop, and inspire a diverse organisation through multiple levels of leadership.</li>\n<li>Create and execute talent strategies focused on workforce planning, capability development, succession planning, and employee engagement.</li>\n<li>Foster a culture of collaboration, innovation, accountability, and continuous learning.</li>\n</ul>\n<p><strong>Capacity Planning &amp; Resource Management</strong></p>\n<ul>\n<li>Oversee organisational design, staffing strategies, and capacity planning activities.</li>\n<li>Monitor workforce utilisation and resource allocation to optimise delivery effectiveness and operational efficiency.</li>\n</ul>\n<p><strong>Stakeholder Management</strong></p>\n<ul>\n<li>Build strong relationships with executive leaders, cross-functional stakeholders, and global technology partners.</li>\n<li>Act as a trusted advisor to senior leadership on engineering performance, talent strategy, and organisational effectiveness.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required)</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in Computer Science, Engineering, Information Systems, or a related field required.</li>\n<li>Minimum of 12 years of progressive experience within software engineering, technology, or digital organisations.</li>\n<li>Minimum of 7 years of leadership experience managing large engineering teams.</li>\n</ul>\n<p><strong>Preferred Qualifications Include</strong></p>\n<ul>\n<li>Master&#39;s degree in Computer Science, Engineering, Information Systems, Business Administration, or a related discipline.</li>\n<li>Experience leading large, globally distributed engineering organisations.</li>\n<li>Demonstrated success serving as a site leader or senior location leader.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Director--Technology-Engineering---Site-Lead_265784","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Director--Technology-Engineering---Site-Lead_265784","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Computer Science","Engineering","Information Systems","AI-assisted software engineering","Agile delivery practices","DevOps principles"],"x-skills-preferred":["Master's degree in Computer Science","Experience leading large, globally distributed engineering organisations","Cloud adoption","Platform engineering","Digital enablement initiatives"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-02T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Computer Science, Engineering, Information Systems, AI-assisted software engineering, Agile delivery practices, DevOps principles, Master's degree in Computer Science, Experience leading large, globally distributed engineering organisations, Cloud adoption, Platform engineering, Digital enablement initiatives"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_f843a53d-d82"},"title":"Clinical Research Physician, Dallas Phase I Onsite","description":"<p>Fortrea is hiring a dynamic Clinical Research Physician at our Dallas, TX Phase I site , onsite, full-time, and fully immersed in cutting-edge clinical trials.</p>\n<p>If you&#39;re ready to lead with purpose, grow your expertise, and collaborate with a dynamic team, this role could be your next big move.</p>\n<p><strong>Role Highlights:</strong></p>\n<ul>\n<li>Support healthy volunteers by providing onsite medical coverage and oversight</li>\n<li>Excellent work/life balance</li>\n<li>M-F schedule 7:30am – 3:30pm schedule variable based on enrollment periods</li>\n<li>Call Rotation 1:4 (every fourth weekend – from home / come in as needed)</li>\n<li>Communicate across clinical teams, regulatory bodies &amp; 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candidates</li>\n<li>Participate in identification and implementation of solutions to local and regional data management issues and concerns</li>\n<li>Assist with quality management activities according to Global data management Plans and Quality Management (QM) Plans</li>\n<li>Support locally based project staff on achieving client satisfaction through delivery of quality data, on-time, and on-budget</li>\n<li>Assist with development and execution of training programs and ensure staff achievement of position competencies</li>\n<li>Support development of global, harmonized SOPs and specific quality processes and procedures</li>\n<li>Identify and implement process improvement solutions and ensure revenue and operating margin performance of the group</li>\n<li>Create action plans to address staff quality and performance issues</li>\n<li>Manage utilization and billability of staff, planning for resource allocation, recruitment, and providing support to Business 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Manager--EDS--External-Data-Specialist-_265779","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Manager--EDS--External-Data-Specialist-_265779","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical data management","ICH/GCP Guidelines","resource management","time and cost estimate development","prioritisation"],"x-skills-preferred":["Life Science","Pharmacy","allied health profession","clinical trial 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query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management</li>\n<li>Assist with training of new employees, e.g. co-monitoring</li>\n<li>Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned</li>\n<li>Perform other duties as assigned by management</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)</li>\n<li>4+ years of Clinical Monitoring experience</li>\n<li>30-50% overnight travel</li>\n</ul>\n<p><strong>Work Environment</strong></p>\n<ul>\n<li>Work is performed in an office environment with exposure to electrical office equipment.</li>\n<li>Frequent travel to clients/ site locations with occasional travel both domestic and international.</li>\n</ul>\n<p><strong>Physical Requirements</strong></p>\n<ul>\n<li>Ability to sit for extended periods and operate a vehicle safely.</li>\n<li>Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.</li>\n<li>Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.</li>\n<li>Ability to access and use a variety of computer software developed both in-house and off-the-shelf.</li>\n<li>Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.</li>\n<li>Regular and consistent attendance.</li>\n<li>Varied hours may be required.</li>\n<li>Target Pay Range: $125 - $142K</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Colorado/FSP-Sr-Clinical-Research-Associate-II---Denver--CO---Oncology_264640","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Colorado/FSP-Sr-Clinical-Research-Associate-II---Denver--CO---Oncology_264640","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$125 - $142K","x-skills-required":["Clinical Monitoring","Clinical Trials","Case Report Forms (CRFs)","Serious Adverse Event (SAE) reporting"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote Colorado"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Monitoring, Clinical Trials, Case Report Forms (CRFs), Serious Adverse Event (SAE) reporting","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":142000,"maxValue":142000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e7e9c1ad-2d1"},"title":"Project Coordinator-I","description":"<p>The Project Management Academy (PM Academy) at Fortrea is seeking a Project Coordinator-I to support project leads in a face-to-face, continuous learning environment. 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decommissioning/archiving tasks and generating reports</li>\n<li>Perform other duties as assigned by study and/or Line Manager</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Currently enrolled as a student at Universidad Panamericana, Universidad Intercontinental, or Tecnologico de Monterrey</li>\n<li>Studying a relevant field, such as engineering, computing, math, computer science, programming, statistics, or public health</li>\n<li>English language proficiency (written and oral)</li>\n<li>Demonstrated ability to organise and communicate effectively</li>\n<li>Attention to detail and ability to work well with others</li>\n<li>Ability to deliver high-quality work</li>\n<li>Familiarity with computer and departmental tools</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Working towards a Bachelor&#39;s or Master&#39;s degree in a Life Science subject</li>\n<li>Experience delivering multiple projects in an academic setting</li>\n<li>Ability to collaborate with various stakeholders and internal/external colleagues</li>\n<li>Additional languages</li>\n</ul>\n<p>Physical Demands/Work Environment:</p>\n<ul>\n<li>Office and/or home-based work environment</li>\n<li>May require overtime and weekend work as required</li>\n<li>Flexible shifts as per business requirements</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Mexico-City/Statistical-Programmer--Internship_265103","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Mexico-City/Statistical-Programmer--Internship_265103","x-work-arrangement":null,"x-experience-level":null,"x-job-type":"internship","x-salary-range":null,"x-skills-required":["data management","regulatory compliance","good clinical 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required</li>\n<li>Support sponsor visits and interactions in collaboration with operations and client management</li>\n<li>Promote and maintain a safe working environment; recommend improvements as appropriate</li>\n<li>Attend investigator meetings as needed</li>\n<li>Serve as an educational resource, trainer, and mentor to staff</li>\n<li>Perform additional duties as assigned</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Graduate of an accredited Nurse Practitioner program</li>\n<li>Current NP certification and active licensure</li>\n<li>Equivalent combination of education and relevant experience may be considered</li>\n<li>Strong English communication skills (spoken and written)</li>\n</ul>\n<p><strong>Experience:</strong></p>\n<ul>\n<li>3–5 years of relevant clinical experience</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Work is performed in a clinical and/or laboratory environment with potential exposure to biological, 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madison/Nurse-Practitioner--NP----Onsite-Madison--WI-Phase-I-Site_265337","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madison/Nurse-Practitioner--NP----Onsite-Madison--WI-Phase-I-Site_265337","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"part-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","FDA regulations","ICH regulations","clinical trials","participant assessment","regulatory 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resources</li>\n<li>Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and feasibility survey</li>\n<li>Remote Pre-Study Visits and follow up documentation, including visit preparation, trip report completion, and other documentation as required to support site selection in line with sponsor, protocol, local and country regulations and requirements</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials</li>\n<li>Collect, track and perform a quality review of all essential documents required for effective and compliant study site activation from Site outreach, submissions, greenlight and until site activation</li>\n<li>Actively participate in team meetings to facilitate study progress and implement action plans for site level risks, underperforming sites, or issues impacting project milestones and escalate issues in a timely manner</li>\n<li>Support the CRA team in preparing for site initiation visits (SIVs) by coordinating with vendors, supplies teams, and study leads to ensure timely distribution of clinical study supplies, accesses and documents per study team guidance</li>\n<li>Responsible for submissions to and liaise with applicable IRB/IEC, Third Bodies (if applicable), and Regulatory Authorities by collaborating with Global Regulatory Submissions Lead (GRSL)</li>\n<li>Perform initial contract and budget negotiations with the sites, as well as amended where applicable</li>\n<li>Ensure high quality documents are filed in applicable systems in accordance with SOPs and project requirements and that the Trial Master File (TMF) is updated and audit ready at all times</li>\n<li>Track the progress of the start-up process and ensure that the research site meets all requirements and deadlines</li>\n<li>Ensure Fortrea is audit ready by completing accurate, timely, and consistent system compliance on an ongoing basis</li>\n<li>Serve as primary contact for investigative sites and 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Site-Navigator-II--Study-Start-up-Specialist----we-re-growing-the-team_265937","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Site-Navigator-II--Study-Start-up-Specialist----we-re-growing-the-team_265937","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH/GCP guidelines","RA","IRB/IEC regulations","clinical research","site management","regulatory compliance"],"x-skills-preferred":["scientific degree","clinical expertise","contract/budgets 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You will be responsible for the full cycle of Clinical Data Management queries, from being in full leadership of your own studies and being the main point of contact with the client, to the most hands-on tasks such as creating eCRFs, cleaning data, and performing independently set-up to close-outs duties.</p>\n<p><strong>What you can expect from us</strong></p>\n<ul>\n<li>Office based or home based anywhere in the listed countries</li>\n<li>Rewarding and meaningful work in an established, diverse, highly profitable and respected global company</li>\n<li>Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances, etc.</li>\n<li>A genuine work-life balance</li>\n<li>Flexibility in working hours</li>\n<li>A thorough onboarding with support from your personal mentor</li>\n<li>A permanent employment contract with Fortrea Drug Development and a rewarding career progression</li>\n</ul>\n<p><strong>Your responsibilities</strong></p>\n<ul>\n<li>Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project. Takes global accountability and serves as the second line of contact at the project level</li>\n<li>Lead studies including a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines. Ability to organize and effectively prioritize workload and deliverables</li>\n<li>Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level. Management and oversight of vendor contracts, resourcing and budget management and oversight of vendor performance for assigned programs, and projects</li>\n<li>Communicates and negotiates effectively with all other Program level team members. Primary point of contact for Clinical Data Management (CDM)</li>\n<li>Demonstrates a business understanding of the compound profile to identify and assist in successful application of consistent CDM processes and documentation across assigned programs</li>\n<li>Provide oversight and expertise of external service providers or in-house teams to deliver quality data with compliance to study model procedures and standards; give guidance on company standards, processes, systems and expectations to external partners, internal partners and third-party vendors</li>\n<li>Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology</li>\n<li>Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards</li>\n<li>Specialist in TA specific data capture and standards, conducts lessons learned and disseminate across the organization as appropriate</li>\n<li>May act as a team leader or mentor Clinical Data Management colleagues and any stakeholder with operational processes used in studies and projects</li>\n<li>Demonstrates willingness to take on and lead any project level activity consistent with current or experience in support of study delivery</li>\n</ul>\n<p><strong>Your profile</strong></p>\n<ul>\n<li>University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution</li>\n<li>8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience. Proven experience in handling customer negotiations and experience with managing Scope of Work and budgets</li>\n<li>Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting</li>\n<li>Excellent oral and written communication and presentation skills</li>\n<li>In-depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations</li>\n<li>Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies</li>\n<li>Ability to lead teams by example on project strategies and achievement of department goals, objectives, and initiatives and to encourage team members to seek solutions</li>\n<li>Demonstrated managerial and interpersonal skills</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Clinical-Data-Manager---sponsor-dedicated_265954","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://www.fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Clinical-Data-Manager---sponsor-dedicated_265954","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical data management","leadership","communication","project management","CDASH","SDTM"],"x-skills-preferred":[],"x-benefits":["pension","health_insurance"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-07T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical data management, leadership, communication, project management, CDASH, SDTM"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_292a1843-19c"},"title":"Clinical Project Manager","description":"<p>Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in Oncology. 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certification, medical or laboratory technology.</li>\n<li>Strong background in clinical research, including several years of experience working on drugs trials and interventional studies.</li>\n<li>At least 1-2 years experience in clinical project management within a CRO or Sponsor environment.</li>\n<li>Ability to lead teams, communicate effectively, and solve problems proactively.</li>\n<li>Excellent German and English skills verbal and written.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Home-Based role with flexible working arrangement.</li>\n<li>Opportunities for professional development, mentorship, and career progression.</li>\n<li>Work with an industry-leading sponsor and expand your leadership capabilities.</li>\n<li>Thanks to our ERGs (Employee Resource Groups), join diverse communities that foster inclusion, professional development, and networking.</li>\n<li>Access to mental health support, wellness initiatives, and fitness programs.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Munich/Sponsor-Dedicated-Local-Trial-Manager-based-in-Germany_2446090","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Munich/Sponsor-Dedicated-Local-Trial-Manager-based-in-Germany_2446090","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical project management","GCP","ICH guidelines","German EU regulatory requirements","life science","clinical research","team 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respiratory therapeutic expertise, ideally including asthma, COPD, ILD, severe respiratory disease, pulmonary fibrosis, or related indications.</p>\n<p>The successful candidates will have experience leading global Phase II and III studies within a CRO or sponsor environment, and demonstrated ability to manage complex, multi-country clinical trials including oversight of timelines, budgets, risks, resources, and sponsor relationships.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Managing complex, multi-country clinical trials</li>\n<li>Overseeing timelines, budgets, risks, resources, and sponsor relationships</li>\n<li>Serving as primary client contact and leading cross-functional global teams</li>\n<li>Operating independently and managing complex stakeholder environments</li>\n<li>Overseeing complex respiratory endpoint vendors</li>\n</ul>\n<p>Preferred experience includes:</p>\n<ul>\n<li>Overall Respiratory expertise including rare respiratory (IPF) and specialized respiratory populations</li>\n<li>Large global programs with accelerated timelines and high enrollment demands</li>\n<li>RBQM and risk-based delivery approaches</li>\n<li>Bid defense, proposal strategy, and client governance experience</li>\n<li>Previous leadership or mentoring responsibilities for PMs and junior team members</li>\n<li>Exposure to decentralized, digital, or innovative trial delivery models</li>\n</ul>\n<p>We are looking for individuals who demonstrate:</p>\n<ul>\n<li>Strong sponsor-facing presence</li>\n<li>Strategic problem-solving and proactive risk management</li>\n<li>Ability to lead through complexity and change</li>\n<li>Commercial awareness and growth mindset</li>\n<li>Collaborative leadership style aligned with our &quot;PM as CEO&quot; operating philosophy</li>\n</ul>\n<p>Qualifications include:</p>\n<ul>\n<li>University/college degree (life science preferred) or certification in a related allied health profession</li>\n<li>Fortrea may consider relevant and equivalent experience in lieu of educational requirements</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Master’s or other advanced degree</li>\n<li>PMP certification</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Poland/Global-Project-Managers---Senior-Project-Managers---Respiratory_265961","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Remote-Poland/Global-Project-Managers---Senior-Project-Managers---Respiratory_265961","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["respiratory therapeutic expertise","clinical trials management","ICH-GCP","study start-up","enrollment management","vendor oversight"],"x-skills-preferred":["rare respiratory populations","large global programs","RBQM","risk-based delivery approaches","bid defense","proposal strategy","client governance","leadership","mentoring","decentralized trials","digital trials","innovative trial delivery models"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-07T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote Poland"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"respiratory therapeutic expertise, clinical trials management, ICH-GCP, study start-up, enrollment management, vendor oversight, rare respiratory populations, large global programs, RBQM, risk-based delivery approaches, bid defense, proposal strategy, client governance, leadership, mentoring, decentralized trials, digital trials, innovative trial delivery models"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_6895f5bb-ad9"},"title":"Hosting Architect","description":"<p>The Hosting Architect will lead Fortrea&#39;s enterprise transition from on-premises data centres to Hyperscaler, delivering a modern, resilient, and automated hosting platform that accelerates application delivery and business innovation.</p>\n<p>This role owns the target-state Azure and hybrid hosting architecture, governs large-scale cloud migration, and modernises operations through automation, Infrastructure as Code, and AI-driven operations.</p>\n<p><strong>Responsibilities:</strong></p>\n<p><strong>Cloud Migration &amp; Hybrid Architecture</strong></p>\n<ul>\n<li>Define and own Fortrea&#39;s target-state Cloud hosting architecture aligned to business and technology strategy.</li>\n<li>Design and govern hybrid architectures during phased migration from on-premises to Cloud.</li>\n<li>Lead workload migration strategies (rehost, re-platform, refactor, retire) to balance speed, risk, and value.</li>\n<li>Act as the architectural authority for hosting and Cloud migration decisions.</li>\n</ul>\n<p><strong>Cloud Platform &amp; Cloud-Native Enablement</strong></p>\n<ul>\n<li>Architect Cloud platforms including landing zones, identity, networking, security, HA, and DR.</li>\n<li>Establish standardised Cloud reference architectures and blueprints to accelerate application onboarding.</li>\n<li>Enable self-service, repeatable platforms that reduce delivery lead time for application and product teams.</li>\n<li>Drive adoption of cloud-native services to simplify operations and improve scalability and cost efficiency.</li>\n</ul>\n<p><strong>Automation, IaC &amp; AI-Led Operations</strong></p>\n<ul>\n<li>Implement an automation-first operating model across hybrid and Cloud environments.</li>\n<li>Build and govern Infrastructure-as-Code using Terraform, ARM/Bicep, PowerShell, Python, or Ansible.</li>\n<li>Introduce AIOps and intelligent automation for predictive monitoring, self-healing, and faster incident resolution.</li>\n<li>Reduce environment provisioning time, manual effort, and operational cost through standardisation and automation.</li>\n</ul>\n<p><strong>Operational Excellence, Resilience &amp; Governance</strong></p>\n<ul>\n<li>Embed resiliency, observability, and reliability engineering into all hosting designs.</li>\n<li>Improve platform availability, reduce incidents, and optimise recovery objectives (RTO/RPO).</li>\n<li>Ensure hosting platforms meet security, audit, and regulatory requirements.</li>\n<li>Provide architectural leadership across infrastructure, application, security, and compliance teams.</li>\n</ul>\n<p><strong>Value &amp; Outcomes</strong></p>\n<ul>\n<li>Faster and safer Cloud migration at enterprise scale.</li>\n<li>Reduced time-to-provision and change lead times for applications.</li>\n<li>Improved platform reliability, availability, and recovery performance.</li>\n<li>Measurable reduction in hosting OPEX through automation and cloud optimisation.</li>\n<li>Hosting platforms that accelerate business capability delivery, not constrain it.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in computer science, Computer Engineering, or a related field.</li>\n<li>Excellent communication and public speaking skills, with the ability to present complex architectural concepts to senior leadership, technical teams, and non-technical stakeholders.</li>\n</ul>\n<p><strong>Required skills (Minimum Required):</strong></p>\n<ul>\n<li>10+ years in hosting, infrastructure, or cloud architecture roles.</li>\n<li>Proven leadership of large-scale Cloud migration programs.</li>\n<li>Strong foundation in enterprise datacentre technologies and hybrid architectures.</li>\n<li>Deep hands-on experience with Cloud compute, networking, storage, identity, and security.</li>\n<li>Experience designing hybrid connectivity and phased migration strategies.</li>\n<li>Strong experience with Infrastructure-as-Code and scripting.</li>\n<li>Exposure to AIOps or intelligent automation platforms.</li>\n<li>Demonstrated success in reducing operational effort and cost through automation.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Hosting-Architect_261449","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Hosting-Architect_261449","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Cloud architecture","Hybrid architecture","Cloud migration","Automation","Infrastructure as Code","AIOps","Cloud computing","Networking","Security","Python","PowerShell","Terraform","ARM/Bicep","Ansible"],"x-skills-preferred":["Cloud architecture certification","Security 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Masters) preferred</li>\n<li>1-2 years of narrative writing experience</li>\n<li>Excellent command of written and spoken English</li>\n<li>Good written and verbal communication skills</li>\n<li>Knowledge of MS Word</li>\n<li>Good organisational and time management ability</li>\n<li>Excellent interpersonal skills</li>\n<li>Scientific or Clinical research experience desirable</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Medical-Writer---Narratives_262636","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Medical-Writer---Narratives_262636","x-work-arrangement":null,"x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MS Word","written and spoken English","organisational skills","time management","interpersonal skills"],"x-skills-preferred":["Scientific or Clinical research experience","advanced 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for:</p>\n<ul>\n<li>Conducting site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Preparing and implementing project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensuring the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguarding data integrity through source document review, source document verification, query generation, and resolution</li>\n<li>Confirming Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current</li>\n<li>Guaranteeing that the study Investigational Product inventory and accountability is accurate</li>\n<li>Ensuring adherence to global quality control and CRA performance metrics</li>\n<li>Ensuring audit readiness at site level</li>\n<li>Acting as a Lead CRA as assigned</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A 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attention to detail, methodical approach to work, and good understanding of medical and clinical research terminology</li>\n</ul>\n<p>The physical demands of this role include:</p>\n<ul>\n<li>Sitting at a computer for long periods of time</li>\n<li>Using hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment (administrative only)</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours as required by the role</li>\n<li>Travel Requirement is 60% of the time (traveling to study sites)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSO-CRA-Shenyang-Zhengzhou-Changchun-_256193","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSO-CRA-Shenyang-Zhengzhou-Changchun-_256193","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Clinical Monitoring","Source Document Review","Data Integrity","Regulatory Compliance"],"x-skills-preferred":["Fortrea SOPs","Phase I monitoring","Life Science or Nursing qualification","e-clinical systems","CTMS"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-08T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Beijing"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, Clinical Monitoring, Source Document Review, Data Integrity, Regulatory Compliance, Fortrea SOPs, Phase I monitoring, Life Science or Nursing qualification, e-clinical systems, CTMS"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_10dbd6f8-db0"},"title":"PSS Project Manager","description":"<p>We are seeking a PSS Project Manager to oversee the delivery of pharmacovigilance services to clients.</p>\n<p>The successful candidate will be responsible for managing client or project specific PSS operations, including adverse event processing and reporting.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Providing leadership and management of global or regional projects</li>\n<li>Monitoring and managing workflow to ensure deadlines are met and safety reporting is compliant with regulations</li>\n<li>Making decisions regarding adverse event reporting</li>\n<li>Working closely with clinical operations and project management groups</li>\n<li>Overseeing the receipt and processing of adverse event reports</li>\n<li>Preparing safety presentations and reports</li>\n<li>Maintaining a strong understanding of safety database conventions and system functionality</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A degree in a life science or related field</li>\n<li>3-7 years of experience in pharmacovigilance or a related field</li>\n<li>Knowledge of worldwide pharmacovigilance regulations and guidelines</li>\n<li>Good communication and leadership skills</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>EudraVigilance certification</li>\n<li>Knowledge of medical device reporting</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/Project-Manager-Drug-Safety_265958","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/Project-Manager-Drug-Safety_265958","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["pharmacovigilance","adverse event reporting","safety management","regulatory compliance","leadership","communication"],"x-skills-preferred":["EudraVigilance certification","medical device 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We are currently proactively engaging with talented CRAs for anticipated upcoming opportunities in FSPx and future growth within our teams.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Manage clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements</li>\n<li>Conduct site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Prepare and implement project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguard data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines</li>\n<li>Confirm Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial</li>\n<li>Guarantee that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements</li>\n<li>Ensure adherence to global quality control and CRA performance metrics</li>\n<li>Ensure audit readiness at site level</li>\n<li>Act in the project role of a Lead CRA as assigned</li>\n</ul>\n<p><strong>General On-Site Monitoring Responsibilities:</strong></p>\n<ul>\n<li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study</li>\n<li>Perform eligibility review, verify that screening, informed consent procedures, and protocol requirements are adhered to according to applicable regulatory requirements</li>\n<li>Ensure the integrity of the source data reported by careful source document review</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance</li>\n<li>Identify deficiencies, deviations, and discrepancies, and initiate corrective action as required</li>\n<li>Perform required monitoring tasks in an efficient manner, according to SOPs and established guidelines</li>\n<li>Travel, including air travel, may be required and is an essential function of the job</li>\n<li>Prepare and submit accurate and timely trip reports</li>\n<li>Independently perform eCRF review, 100% source data verification, query generation, and resolution against established data review guidelines</li>\n<li>Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation, and site management</li>\n<li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems</li>\n<li>Track IP shipments and supplies, as needed</li>\n<li>Track and follow-up on serious adverse events as assigned</li>\n<li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met</li>\n<li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned</li>\n<li>Attend investigators&#39; meetings, project team meetings, and teleconferences, and others as needed</li>\n<li>Present training content for site initiation</li>\n<li>Assist with training of new employees</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements</li>\n<li>Thorough knowledge of monitoring procedures</li>\n<li>Basic understanding of the clinical trial process</li>\n<li>Fluent in local office language and in English, both written and verbal</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution</li>\n<li>A minimum of 1.5 years of Clinical Monitoring experience</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines</li>\n<li>Ability to work with minimal supervision</li>\n<li>Understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives, and follow-up of SAEs</li>\n<li>Good planning, organization, and problem-solving abilities</li>\n<li>Works efficiently and effectively in a matrix environment</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Must be able to sit at a computer for long periods of time</li>\n<li>Must be able to use hands to finger, handle, or touch objects, tools, or controls, including a computer keyboard, for up to 8 hours per day</li>\n<li>Standard office and/or home working environment</li>\n<li>Clinical Research Unit and hospital environment (administrative only)</li>\n<li>Risk of eye strain</li>\n<li>Will involve outside of normal office hours as required by the role</li>\n<li>Travel Requirement is 60% of the time (traveling to study sites)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/CRA-I-CRA-II_265799","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/CRA-I-CRA-II_265799","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Clinical Monitoring","Source Document Review","Data Integrity","Regulatory Requirements","English"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-08T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, Clinical Monitoring, Source Document Review, Data Integrity, Regulatory Requirements, English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_49bafee1-ecc"},"title":"Clinical Research Associate II (CRA2)","description":"<p>We&#39;re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a meaningful impact in healthcare.</p>\n<p>As a CRA2, you will play a key role in managing and monitoring clinical trials, ensuring compliance with regulatory requirements, and fostering strong relationships with investigative sites. This is a fantastic opportunity for professionals looking to grow their career in a dynamic and collaborative environment.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Site management responsibility for clinical studies according to Fortrea&#39;s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.</li>\n<li>Conducts site monitoring responsibilities for clinical trials according to Fortrea&#39;s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.</li>\n<li>Prepares and implements project plans related to Clinical Monitoring responsibilities.</li>\n<li>Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.</li>\n<li>Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.</li>\n<li>Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.</li>\n<li>Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.</li>\n<li>Ensures adherence to global quality control and CRA performance metrics.</li>\n<li>Ensures audit readiness at site level.</li>\n<li>Acts in the project role of a Lead CRA as assigned.</li>\n</ul>\n<p><strong>General On-Site Monitoring Responsibilities:</strong></p>\n<ul>\n<li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study.</li>\n<li>Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.</li>\n<li>Ensure the integrity of the source data reported by careful source document review.</li>\n<li>Monitor data for missing or implausible data.</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.</li>\n<li>Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines.</li>\n<li>Travel, including air travel, may be required and is an essential function of the job.</li>\n<li>Prepare and submit accurate and timely trip reports.</li>\n<li>Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.</li>\n<li>Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management.</li>\n<li>Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.</li>\n<li>Track IP shipments and supplies, as needed.</li>\n<li>Track and follow-up on serious adverse events as assigned.</li>\n<li>Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.</li>\n<li>Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.</li>\n<li>Attend investigators&#39; meetings, project team meetings and teleconferences, and others as needed.</li>\n<li>Present training content for site initiation.</li>\n<li>Assist with training of new employees.</li>\n</ul>\n<p><strong>Qualifications (Minimum Required):</strong></p>\n<ul>\n<li>University or college degree, or certification in a related allied health profession from an appropriately accredited institution.</li>\n<li>Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.</li>\n<li>Thorough knowledge of monitoring procedures.</li>\n<li>Basic understanding of the clinical trial process.</li>\n<li>Fluent in local office language and in English, both written and verbal.</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>Typically 2 years of onsite clinical monitoring experience.</li>\n<li>Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.</li>\n<li>Ability to work with minimal supervision.</li>\n<li>Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.</li>\n<li>Good planning, organization, and problem-solving abilities.</li>\n<li>Works efficiently and effectively in a matrix environment.</li>\n</ul>\n<p><strong>Physical Demands/Work Environment:</strong></p>\n<ul>\n<li>Location: Incumbent of the role needs to be based in Melbourne, Adelaide or Perth.</li>\n<li>Will involve outside of normal office hours as required by the role.</li>\n<li>Travel Requirement is 60% of the time (traveling to study sites).</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Melbourne/Clinical-Research-Associate-II---Melbourne--Adelaide--or-Perth_261586","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Melbourne/Clinical-Research-Associate-II---Melbourne--Adelaide--or-Perth_261586","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","clinical trial process","monitoring procedures","English"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-09T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Melbourne"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH GCP Guidelines, clinical trial process, monitoring procedures, English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_07defa76-eba"},"title":"EDC Design and Specifications Lead","description":"<p>We are seeking an experienced EDC Design and Specifications Lead to join our team. As an EDC Design and Specifications Lead, you will be responsible for delivering EDC design and specifications within the scope of assigned projects to achieve project integrity and the delivery of on-time, quality data.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Design and develop EDC systems, including Rave, Veeva, Inform, and other EDC systems</li>\n<li>Prepare and review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency</li>\n<li>Participate in sponsor meetings and audits/inspections</li>\n<li>Assign tasks and responsibilities to team members and optimize team capability</li>\n<li>Assist Managers in data collection for productivity, Quality, timelines, and resource planning</li>\n<li>Perform quality control procedures for specification development</li>\n<li>Conduct team meetings and provide guidance to Programmers and Data managers</li>\n<li>Maintain study specifications for assigned projects</li>\n<li>Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills</li>\n<li>Advance competency through participation in internal and external professional seminars and symposiums</li>\n<li>Conduct Quality Control of study design for assigned projects</li>\n<li>Participate in the validation of EDC studies when requested</li>\n<li>Create and maintain library objects within the Global Libraries</li>\n<li>Ensure compliance of standard objects usage throughout the business</li>\n<li>Manage standard objects within the Global Libraries</li>\n<li>Perform all activities related to specification development for study build and design of databases according to Standard procedures</li>\n<li>Review and approve derivations and edit checks requested by project teams</li>\n<li>Mentor study teams in CRF Design and specification development for leading EDC databases</li>\n<li>Oversee project work of junior staff</li>\n<li>Mentor and aid in staff development, and achievement of competency standards</li>\n<li>Assist with the development of training programs to ensure staff, project, and technical achievement of position competencies</li>\n<li>Present training programs to technical staff regarding study build, standards maintenance, and/or change control</li>\n<li>Participate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activities</li>\n<li>Notify project leadership of requests for out-of-scope work and advise management of changes in scope of projects</li>\n<li>Complete work according to Fortrea SOPs, Work Instructions, and project-specific guidelines in accordance with Good Clinical Practice</li>\n<li>Meet with data managers on assigned projects to discuss technical strategies, contractual obligations, and timelines</li>\n<li>Provide consultation in database design and development with data managers</li>\n<li>Participate in the ongoing review of processes to ensure adaptation of best practices</li>\n<li>Assist management with evaluation of new technologies as assigned</li>\n<li>Prioritize personal workload to meet specified completion dates and perform work with minimal direction</li>\n<li>Provide feedback to management if any action is needed to increase utilization, improve efficiency, or amend resource levels required on a project</li>\n<li>Participate in the validation of new or updates to software</li>\n<li>Provide expert guidance to project teams, external clients, and internal clients within a global setting</li>\n<li>Provide feedback to management on the development potential of staff to assist in staff development</li>\n<li>Maintain awareness of new developments in EDC vendor products which may be applied to improve efficient use of these systems</li>\n<li>Implement processes as they are refined, or as new processes are developed and initiate and participate in ongoing review of processes to ensure continual improvement</li>\n<li>Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance</li>\n<li>Perform other duties as assigned</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University/college degree in life sciences, health sciences, information technology, or related subjects preferred</li>\n<li>Minimum 6 years of relevant work experience, including data management and/or database programming and spec Design activities, including 4 years in Medidata RAVE, Oracle Inform, Veeva Vault, or equivalent EDC experience</li>\n<li>Fluent in English, both written and verbal</li>\n<li>Demonstrate excellent problem-solving skills, a proactive approach, and ability to make sound decisions</li>\n<li>Demonstrated skill in leading teams, by example and mentoring staff</li>\n<li>Excellent oral and written communication and presentation skills</li>\n<li>Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC</li>\n<li>Working knowledge of relationship and regulatory obligation of CRO industry with pharmaceutical/biotechnological companies</li>\n<li>Demonstrated ability to work in a team environment</li>\n<li>Demonstrated ability to handle multiple competing priorities</li>\n<li>Proven interpersonal skills</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Senior-Technical-Designer_265481","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Bangalore/Senior-Technical-Designer_265481","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["EDC design","specifications development","data management","database programming","CRF/eCRF 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requirements.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits</li>\n<li>Prepare and implement project plans related to Clinical Monitoring responsibilities</li>\n<li>Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to</li>\n<li>Safeguard data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines</li>\n<li>Confirm Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial</li>\n<li>Guarantee that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements</li>\n<li>Ensure adherence to global quality control and CRA performance metrics</li>\n<li>Ensure audit readiness at site level</li>\n<li>Act in the project role of a Lead CRA as assigned</li>\n</ul>\n<p>General On-Site Monitoring Responsibilities:</p>\n<ul>\n<li>Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study</li>\n<li>Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to</li>\n<li>Ensure the integrity of the source data reported by careful source document review</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Ensure study data completeness, accuracy, consistency, and compliance</li>\n<li>Identify deficiencies, deviations and discrepancies, and initiate corrective action as required</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>University or college degree, or certification in a related allied 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This includes verifying study training records, conducting site initiation visits, routine monitoring, and close-out visits. 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/CRA-II---Sr-CRA_254296-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/CRA-II---Sr-CRA_254296-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH GCP Guidelines","Clinical Monitoring","Regulatory Requirements","English","Spanish"],"x-skills-preferred":["Fortrea SOPs","Phase I monitoring","Life Science or Nursing qualification","e-clinical 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the start-up phase of a clinical study and potentially through closeout activities as required.</p>\n<p>Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach through to site activation, extending through the maintenance phase of the study as required.</p>\n<p>A crucial component in meeting the requirements of the Site Navigator role is ensuring regulatory compliance, robust site management, optimal site support and training, and effective collaboration between the sponsor, CRO, and clinical site staff.</p>\n<p><strong>Summary of Responsibilities:</strong></p>\n<ul>\n<li>Oversight of site level tasks associated with efficient site activation in accordance with ICH/GCP guidelines, local regulations, SOPs and project requirements, including collaboration with project leadership and local monitors to collaboratively achieve project milestones while also ensuring Study Participant rights, wellbeing and safety are protected.</li>\n<li>Identifying potential research sites that align with the study&#39;s criteria and assessing their capabilities and resources.</li>\n<li>Conduct initial site outreach, i.e., site engagement, collection of Confidentiality Agreement, and collection of feasibility survey.</li>\n<li>Apply independent judgment and discretion in managing site-level activities, resolving issues, and making decisions that support study timelines and compliance requirements.</li>\n<li>Remote Pre-Study Visits and follow up documentation, including visit preparation, trip report completion, and other documentation as required to support site selection in line with sponsor, protocol, local and country regulations and requirements.</li>\n<li>Support customization and translation of informed consent forms and patient-facing materials.</li>\n<li>Collect, track and perform a quality review of all essential documents required for effective and compliant study site activation from site outreach, submissions, greenlight and until site activation.</li>\n<li>Actively participate in study team meetings to support study progress, develop and implement action plans for site level risks, underperforming sites, or issues impacting project milestones and escalate issues in a timely manner.</li>\n<li>Support the CRA team in preparing for site initiation visits (SIVs) by coordinating with vendors, supplies teams, and study leads to ensure timely distribution of clinical study supplies, accesses and documents per study team guidance.</li>\n<li>Responsible for submissions to and liaise with applicable IRB/IEC, Third Bodies (if applicable), and Regulatory Authorities by collaborating with Global Regulatory Submissions Lead (GRSL).</li>\n<li>Perform initial contract and budget negotiations with the sites, as well as amended where applicable.</li>\n<li>Ensure high quality documents are filed in applicable systems in accordance with SOPs and project requirements and that the Trial 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certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) or 2-3 years&#39; work experience in clinical research, including a working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations.</li>\n<li>Fortrea may consider relevant and equivalent experience in lieu of educational requirements.</li>\n<li>In lieu of the above requirement, candidates with a High School Diploma or equivalent AND a minimum of 5 years&#39; work experience in clinical research, including a strong working knowledge of the ICH/GCP guidelines and RA, IRB/IEC regulations will be considered.</li>\n<li>Fluent in local official language and in English, both written and verbal.</li>\n</ul>\n<p><strong>Experience (Minimum Required):</strong></p>\n<ul>\n<li>A scientific degree and/ or clinical expertise is optimal for this role.</li>\n<li>At least one year of experience in a related field, (e.g., medical, clinical, pharmaceutical, laboratory research, data analysis, data management or technical writing). One year of clinical research is preferred.</li>\n<li>Basic knowledge of ICH/GCP, RA, IRB/IEC, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites is preferred.</li>\n<li>Demonstrated understanding of research protocol requirements.</li>\n<li>Effective communication with various stakeholders, including site staff, CRO personnel, and regulatory authorities.</li>\n<li>Ability to manage multiple tasks and deadlines simultaneously, ensuring that all requirements are met in a timely manner.</li>\n<li>Understanding of relevant regulations and guidelines related to clinical trials and research.</li>\n<li>Ability to identify and resolve potential issues that may arise during the start-up process.</li>\n<li>Ability to negotiate contracts and budgets effectively with research sites.</li>\n</ul>\n<p><strong>Physical Demands / Work Environment:</strong></p>\n<ul>\n<li>Remote-based work required with possible office presence depending on location.</li>\n<li>Travel requirements: Limited to training only.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/Site-Navigator-I_266081-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/Site-Navigator-I_266081-1","x-work-arrangement":"remote","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["ICH/GCP guidelines","RA","IRB/IEC regulations","clinical research","site management","regulatory compliance"],"x-skills-preferred":["scientific degree","clinical expertise","medical","pharmaceutical","laboratory research","data analysis","data management","technical writing"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-13T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Seoul"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH/GCP guidelines, RA, IRB/IEC regulations, clinical research, site management, regulatory compliance, scientific degree, clinical expertise, medical, pharmaceutical, laboratory research, data analysis, data management, technical writing"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_00481bbe-07a"},"title":"FSP Clinical Project Coordinator","description":"<p>We are seeking a detail-oriented and organised individual to join our team as an FSP Clinical Project Coordinator. 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This is a sponsor-dedicated, office-based position in Vienna, offering exposure to global clinical development.</p>\n<p><strong>Key Responsibilities</strong> You will:</p>\n<ul>\n<li>Coordinate administrative tasks related to regulatory submissions</li>\n<li>Maintain trackers, logs, and documentation in compliance with internal SOPs and external regulations</li>\n<li>Support preparation and review of study-related documentation</li>\n<li>Liaise with internal teams for timely updates and data accuracy</li>\n<li>Assist in scheduling meetings, managing email communications, and organising project files</li>\n<li>Monitor timelines and escalate delays or issues to relevant stakeholders</li>\n<li>Contribute to continuous improvement of administrative processes</li>\n</ul>\n<p><strong>Required Qualifications</strong></p>\n<ul>\n<li>At least 1 year of work experience in a clinical trial environment</li>\n<li>Some experience in clinical research</li>\n<li>Regulatory administrative 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Vienna/FSP-Clinical-Project-Coordinator-based-in-Vienna_264735-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Vienna/FSP-Clinical-Project-Coordinator-based-in-Vienna_264735-1","x-work-arrangement":"onsite","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Microsoft Office","document management","German","English","regulatory administration"],"x-skills-preferred":["clinical research"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-13T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Vienna"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Microsoft Office, document management, German, English, regulatory administration, clinical research"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_04cfbfc3-e42"},"title":"Senior Manager, IT Quality and Compliance","description":"<p>The Senior Manager, IT Quality and Compliance is a member of the Global IT Quality and Compliance leadership team and assists the Director in executing, managing, and overseeing one or more disciplines of the IT global controls framework.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Lead internal business and IT partners in audits, coordinating IT involvement and ensuring proper follow-up and on-time completion of IT Quality events.</li>\n<li>Coordinate, review, and complete contract reviews, client questionnaires, and compliance initiatives impacting IT.</li>\n<li>Serve as point of contact for IT audit support resources and track audit support metrics.</li>\n<li>Lead the management and execution of one or more components of the overall IT Quality program globally.</li>\n<li>Represent IT Quality on global IT projects and committees, providing subject matter expertise and oversight.</li>\n<li>Triage Audit Quality Events to ensure appropriate IT ownership and monitor IT QEs and CAPAs.</li>\n<li>Recommend proper controls for the Company&#39;s computer systems to ensure application reliability, infrastructure integrity, data integrity, and subject safety.</li>\n<li>Deliver technology, standards, and processes aligned with department objectives and goals.</li>\n<li>Partner 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various validation methodologies and their implementation in an IT organisation.</li>\n<li>Experience working in a team-oriented, collaborative environment.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/Senior-Manager--IT-Quality-and-Compliance_265814","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/Senior-Manager--IT-Quality-and-Compliance_265814","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["audit/compliance","IT","Data Management","validation methodologies","regulatory 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The role involves providing programming for the analysis of RWD from diverse sources, developing analysis-ready datasets, and creating tables/figures/listings (TFLs) from analytic datasets.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Provide programming for the analysis of RWD from diverse sources including observational studies and existing secondary data sources</li>\n<li>Develop analysis-ready datasets from source data, including derivation of analytic variables, following an analytic plan</li>\n<li>Independently develop tables/figures/listings (TFLs) from analytic datasets and following an analytic plan</li>\n<li>Provide programs to validate analysis datasets and results presented in TFLs and resolve discrepancies with minimal oversight</li>\n<li>Create and maintain documentation of programming for assigned deliverables</li>\n<li>Provide quality cross-checks of written deliverables to analytic results</li>\n<li>Communicate accurate and timely status updates to RWE biostatisticians, epidemiologists, and team members</li>\n<li>Provide analytic programming of other data sources for various projects, as needed</li>\n</ul>\n<p><strong>Process Improvement:</strong></p>\n<ul>\n<li>Follow standard operating procedures (SOPs) relevant to assigned projects</li>\n<li>Identify opportunities to enhance productivity, quality, and efficiency in analytic processes</li>\n</ul>\n<p><strong>People:</strong></p>\n<ul>\n<li>Provide informal guidance to Associate, RWD Analysts</li>\n<li>Participate in department meetings to share knowledge and insights</li>\n<li>Maintain a standard of personal behavior and business ethics in line with Fortrea culture</li>\n</ul>\n<p><strong>Business Development:</strong></p>\n<ul>\n<li>Contribute to repeat business through delivery of quality analyses and deliverables</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree in statistics, mathematics, epidemiology, or another relevant field</li>\n<li>≥3 years of health research data analysis experience</li>\n<li>Proficiency in relevant programming language that meets current client demand (e.g., SAS, R, Python)</li>\n<li>Proficiency in SAS macro language</li>\n<li>Working knowledge of Microsoft Word, PowerPoint, and Excel</li>\n<li>Ability to solve problems independently</li>\n<li>Ability to follow defined processes</li>\n<li>Strong attention to detail</li>\n<li>Strong oral and written communication</li>\n<li>Team player mentality</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree or higher with a strong focus in statistics</li>\n<li>Experience conducting analyses of observational study data</li>\n<li>Proficiency in CDISC standards (e.g., writing SDTM and ADaM specifications)</li>\n<li>Experience applying CDISC standards to observational study data</li>\n<li>Analytic experience with existing secondary data sources (e.g., claims, hospital administration, electronic health records, registries)</li>\n<li>Ability to challenge conventional thinking to develop solutions</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Associate-Real-world-Data--RWD--Analyst--EMEA-_264959","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Warsaw/Senior-Associate-Real-world-Data--RWD--Analyst--EMEA-_264959","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["SAS","Python","R","Microsoft Word","PowerPoint","Excel","statistics","mathematics","epidemiology"],"x-skills-preferred":["CDISC standards","SDTM","ADaM specifications","observational study data analysis"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-13T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Warsaw"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Data Science","industry":"Healthcare","skills":"SAS, Python, R, Microsoft Word, PowerPoint, Excel, statistics, mathematics, epidemiology, CDISC standards, SDTM, ADaM specifications, observational study data analysis"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_cdc36d76-f1c"},"title":"Clinical Research Associate","description":"<p>We are seeking a Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for site monitoring and site management for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conduct routine monitoring and closeout of clinical sites</li>\n<li>Maintain study files and conduct pre-study and initiation visits</li>\n<li>Liaise with vendors and perform other duties as assigned</li>\n<li>Ensure study staff have received proper materials and instructions to safely enter patients into the study</li>\n<li>Verify informed consent procedures and protocol requirements are adhered to</li>\n<li>Review source documents to ensure data integrity</li>\n<li>Monitor data for missing or implausible data</li>\n<li>Perform monitoring tasks efficiently and manage travel expenses economically</li>\n<li>Ensure audit readiness at the site level</li>\n<li>Travel may be required, including air travel</li>\n<li>Prepare 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Clinical Team Lead (CTL) owns the clinical delivery of clinical research trials, functioning as the Clinical Project Manager (CPM) within the core project team.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Drive clinical project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.</li>\n<li>Collaborate with clients and project teams across a matrixed, multicultural environment.</li>\n<li>Develop and prioritize clinical project strategies with the project team and stakeholders.</li>\n<li>Manage project operations, including subject recruitment and retention, clinical vendor delivery, and monitoring visit strategies.</li>\n<li>Identify and mitigate clinical project risks using end-to-end risk management practices.</li>\n<li>Utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem-solving.</li>\n<li>Ensure adherence to project governance, professional standards, and 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/Senior-Clinical-Data-Manager_266015","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/Senior-Clinical-Data-Manager_266015","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Data Management","clinical data standards","CDISC","database management software","reporting tools","medical coding systems","eSource","eCOA","eConsent","central monitoring tools","risk-based quality management","RBQM","project management","organizational skills","critical thinking","sound judgement"],"x-skills-preferred":["SCDM Certified Clinical Data Manager","RAVE","eClinical Solutions 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safely.</li>\n<li>Repetitive hand movement and ability to make fast, simple, repeated movements.</li>\n<li>Occasional crouching, stooping, bending, and twisting.</li>\n<li>Light to moderate lifting and carrying.</li>\n</ul>\n<p><strong>Salary:</strong> $100-112K per year</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP-Clinical-Research-Associate-2---Las-Vegas--NV---Oncology_266182","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP-Clinical-Research-Associate-2---Las-Vegas--NV---Oncology_266182","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$100-112K","x-skills-required":["Clinical 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resolution</li>\n<li>Confirming Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current</li>\n<li>Guaranteeing accurate Investigational Product inventory and accountability</li>\n<li>Ensuring adherence to global quality control and CRA performance metrics</li>\n<li>Ensuring audit readiness at site level</li>\n<li>Acting as a Lead CRA as assigned</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A university or college degree, or certification in a related allied health profession</li>\n<li>Thorough understanding of ICH GCP Guidelines and local regulatory requirements</li>\n<li>Thorough knowledge of monitoring procedures</li>\n<li>Basic understanding of the clinical trial process</li>\n<li>Fluent in local office language and in English, both written and verbal</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Thorough working knowledge of Fortrea SOPs for site monitoring</li>\n<li>Additional years of experience in a related 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sites.</p>\n<p>The successful candidate will be responsible for ensuring that studies are conducted according to Company and Sponsor Standard Operating Procedures, as well as Regulatory Guidelines.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Conducting routine monitoring and closeout of clinical sites</li>\n<li>Maintaining study files and conducting pre-study and initiation visits</li>\n<li>Liaising with vendors and other stakeholders</li>\n<li>Ensuring the protection of study patients and the integrity of data submitted</li>\n<li>Monitoring data for missing or implausible entries</li>\n<li>Ensuring audit readiness at the site level</li>\n<li>Preparing accurate and timely trip reports</li>\n<li>Interacting with internal work groups to evaluate needs and resources</li>\n<li>Acting as a contact for clinical trial supplies and other suppliers</li>\n<li>Managing investigator site budgets and tracking Serious Adverse Event reporting</li>\n<li>Performing CRF reviews and query generation</li>\n<li>Assisting with training and development of new employees</li>\n<li>Coordinating designated clinical projects</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A university or college degree in a related field (e.g., nursing, life sciences)</li>\n<li>Basic knowledge of Regulatory Guidelines and the clinical trial process</li>\n<li>Fluent in local office language and English</li>\n<li>Six months of experience in a related role (e.g., site management, study coordinator)</li>\n<li>Good planning, organisation, and problem-solving skills</li>\n<li>Valid Driver&#39;s License</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Additional experience in a related field (e.g., medical, clinical, pharmaceutical)</li>\n<li>On-site monitoring experience</li>\n<li>Understanding of medical and clinical research terminology</li>\n<li>Experience using a clinical trial management system (CTMS)</li>\n</ul>\n<p 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respected global company</li>\n<li>Highly competitive compensation packages, including country-specific benefits and wellbeing programs</li>\n<li>A genuine work-life balance with flexibility in working arrangements</li>\n<li>Comprehensive onboarding and training supported by experienced colleagues and mentors</li>\n<li>Opportunities for continuous learning, professional development and career progression</li>\n</ul>\n<p><strong>Your profile</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Life Sciences, Clinical Research, Information Technology or another related scientific or technical discipline preferred</li>\n<li>Minimum 3–4 years of experience in a clinical research environment, preferably with exposure to Phase I studies</li>\n<li>Understanding of Electronic Data Capture (EDC) systems and the clinical trial process</li>\n<li>Working knowledge of GCP, ICH Guidelines and 21 CFR Part 11 requirements</li>\n<li>Experience working with clinical source documentation and data collection 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Leeds/Intern---Pricing-team_266035","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Fortrea","sameAs":"https://fortrea.com","logo":"https://logos.yubhub.co/fortrea.com.png"},"x-apply-url":"https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Leeds/Intern---Pricing-team_266035","x-work-arrangement":null,"x-experience-level":null,"x-job-type":"internship","x-salary-range":null,"x-skills-required":["life sciences","bio-medical","pharmacy","nursing","medicine","STEM","analytical skills","informatics 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Our Early Careers program is more than an internship , it’s a launchpad for your future.</p>\n<p>As an Intern, you’ll join a global team where curiosity, motivation, and fresh ideas are celebrated. You’ll work on meaningful projects, learn from experienced professionals, and see firsthand how clinical research and healthcare innovation change lives.</p>\n<p>We don’t expect you to know it all. What matters most is your potential, your drive to learn, and your willingness to grow. 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You&#39;ll gain exposure to real clinical trials working alongside experienced Clinical Data Managers and with state-of-the-art technology that will allow you to become an independent Clinical Data Management professional.</p>\n<p>The Clinical Data Management team is pivotal in the management of the whole clinical trials life-cycle and takes care for the development of the project documentation, system set-up, data entry and data validation, data reconciliations, database lock, and many other critical tasks across all phases of the project.</p>\n<p><strong>Internship Opportunity Summary</strong></p>\n<ul>\n<li>Learn from Day One: Embrace a hands-on learning experience from the moment you step in the door. At Fortrea we believe in nurturing talent. You won&#39;t just be a part of our team; you&#39;ll be a vital contributor from your first day, gaining practical insights and real-world skills.</li>\n<li>Global Exposure: Immerse yourself in the world of international clinical research. Collaborate with professionals from diverse cultures and backgrounds, broadening your horizons and enhancing your global perspective.</li>\n<li>Own Your Responsibilities: Take charge of clinical data management processes and witness the impact of your work on pioneering medical studies. 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