{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/at/iqvia-biotech/"},"x-facet":{"type":"company","slug":"iqvia-biotech","display":"IQVIA Biotech","count":25},"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_724c4f38-54b"},"title":"Clinical Research Associate II","description":"<p>IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is home-based in Eastern Canada and requires fluency in both French and English.</p>\n<p>The CRA II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Conduct site selection, initiation, monitoring, and close-out visits</li>\n<li>Train site personnel on study protocols, EDC systems, and study requirements</li>\n<li>Ensure high-quality source documentation, data integrity, and timely query resolution</li>\n<li>Oversee IP accountability and regulatory document collection</li>\n<li>Serve as the primary site contact and maintain regular communication</li>\n<li>Prepare monitoring reports following Standard Operating Procedures and timelines</li>\n<li>Support investigator meetings and collaborate with CTMs/Lead CRAs</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bilingual in French and English (Required)</li>\n<li>Bachelor’s Degree required. Preference in life sciences or related discipline. Equivalent combination of education, training and experience may be accepted in lieu of degree.</li>\n<li>At least 1 year of onsite monitoring experience (Required)</li>\n<li>Ability to travel 65–70%</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $74,700.00 - $124,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Attach-de-recherche-clinique-II--Oncologie--Clinical-Research-Associate-II--Oncology--IQVIA-Biotech_R1565812","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Attach-de-recherche-clinique-II--Oncologie--Clinical-Research-Associate-II--Oncology--IQVIA-Biotech_R1565812","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$74,700.00 - $124,500.00","x-skills-required":["French","English","GCP/ICH guidelines","clinical trial management"],"x-skills-preferred":["life sciences","oncology monitoring experience"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T02:15:44.536Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Research","industry":"Healthcare","skills":"French, English, GCP/ICH guidelines, clinical trial management, life sciences, oncology monitoring experience","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":74700,"maxValue":124500,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_fec13323-1dc"},"title":"Senior Clinical Project Manager or Clinical Project Manager","description":"<p>IQVIA Biotech is seeking an experienced Senior Clinical Project Manager or Clinical Project Manager to drive the successful delivery of clinical trials. As a Senior Clinical Project Manager or Clinical Project Manager, you will lead the planning and execution of global and multi-regional clinical studies from start-up through closeout.</p>\n<p>Key Responsibilities:</p>\n<ul>\n<li>Lead the planning and execution of global and multi-regional clinical studies from start-up through closeout.</li>\n<li>Serve as the primary point of contact for sponsors and maintain strong customer relationships.</li>\n<li>Develop and implement integrated study management plans in collaboration with cross-functional teams.</li>\n<li>Drive study delivery while optimizing timelines, quality, and budget performance.</li>\n<li>Provide strategic leadership for project teams, setting objectives and ensuring accountability for key milestones.</li>\n<li>Identify, assess, and proactively manage project risks, issues, and change requests.</li>\n<li>Monitor project progress and communicate study status, metrics, and key updates to internal and external stakeholders.</li>\n<li>Ensure compliance with applicable regulations, ICH-GCP guidelines, SOPs, and study-specific requirements.</li>\n<li>Support business development activities, including proposal development and bid defense presentations.</li>\n<li>Oversee project financial performance, including forecasting, budget management, and scope change management.</li>\n<li>Mentor and support the development of project team members while fostering collaboration across functions and regions.</li>\n<li>Drive continuous improvement by sharing lessons learned and promoting best practices.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor’s degree in Life Sciences or a related field.</li>\n<li>Minimum of 7 years of clinical research experience, including at least 4 years of clinical project management experience.</li>\n<li>Strong understanding of clinical trial conduct, ICH-GCP, regulatory requirements, and global drug development processes.</li>\n<li>Experience managing small to medium, full-service, multi-country, and/or multi-regional clinical studies.</li>\n<li>Proven ability to lead cross-functional teams and manage complex stakeholder relationships.</li>\n<li>Strong financial acumen with experience managing project budgets, forecasting, and scope changes.</li>\n<li>Excellent communication, presentation, negotiation, and problem-solving skills.</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/XMLNAME--Senior--Clinical-Project-Manager--IQVIA-Biotech_R1571841","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA 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multiple priorities in a fast-paced environment</li>\n<li>Proficiency with Microsoft Office applications and clinical trial systems</li>\n</ul>\n<p>Preferred skills:</p>\n<ul>\n<li>Strong therapeutic area knowledge and protocol management experience</li>\n<li>Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams</li>\n<li>Experience mentoring or supporting the development of junior clinical research professionals</li>\n</ul>\n<p>The potential base pay range for this role is $105,100.00 - $197,500.00 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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Sr-CRA--Oncology--IQVIA-Biotech_R1571573-4","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA 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maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi-protocol programs.</li>\n<li>Collaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements.</li>\n<li>Provide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study start-up and maintenance.</li>\n<li>Create and review scientific, technical, and administrative documentation required for study initiation.</li>\n<li>Assess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company.</li>\n<li>Ensure contracting efficiency, adherence to timelines, and achievement of financial targets.</li>\n<li>Track and report contracting performance metrics and out-of-scope activities.</li>\n<li>Partner with Quality Management to uphold high contract management and quality standards.</li>\n<li>Mentor and coach colleagues, delivering training and technical guidance.</li>\n<li>Present to clients and professional bodies as needed.</li>\n<li>Maintain accurate internal system documentation, including CTMS, trackers, and project plans.</li>\n<li>Build and maintain strong relationships with preferred clients, serving as liaison for key accounts when required.</li>\n</ul>\n<p>Qualifications &amp; Experience:</p>\n<ul>\n<li>Bachelor’s degree in a related field (required).</li>\n<li>5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert.</li>\n<li>Equivalent combinations of education, training, and experience will be considered.</li>\n<li>Strong negotiation and communication skills, with the ability to challenge and influence.</li>\n<li>Excellent interpersonal skills and proven success working within matrix teams.</li>\n<li>Advanced legal, financial, and technical writing abilities.</li>\n<li>Solid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process.</li>\n<li>Knowledge of local and global regulatory requirements, SOPs, and corporate standards.</li>\n<li>Ability to exercise independent judgment and take calculated risks.</li>\n<li>Strong project leadership skills and experience mentoring others.</li>\n<li>Excellent planning, organizational, and presentation skills.</li>\n<li>Strong proficiency in Microsoft Word, Excel, and other Office tools.</li>\n<li>Deep knowledge of clinical trial contract management processes.</li>\n<li>Proven experience leveraging metrics to establish timelines and deliverables.</li>\n<li>Ability to initiate and grow programs across departments to drive organizational impact.</li>\n</ul>\n<p>What We Offer:</p>\n<ul>\n<li>Opportunity to work on global, high-complexity clinical programs.</li>\n<li>A collaborative, supportive, and growth-oriented environment.</li>\n<li>The chance to influence key clients and shape contracting strategy at scale.</li>\n<li>Career progression and professional development opportunities.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Senior-Site-Contracts-Associate--IQVIA-Biotech---Germany_R1566236","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Senior-Site-Contracts-Associate--IQVIA-Biotech---Germany_R1566236","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial contracting","contract management","regulatory requirements","GCP/ICH","Microsoft Office"],"x-skills-preferred":[],"x-benefits":["equity"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-29T21:54:17.268Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Frankfurt, Hesse"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial contracting, contract management, regulatory requirements, GCP/ICH, Microsoft Office"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d8be68b3-ed4"},"title":"CRA 2","description":"<p>IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a minimum of 1 year of on-site monitoring experience and oncology solid tumor monitoring experience.</p>\n<p>We are seeking a dedicated Clinical Research 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In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Conduct all types of site visits,selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.</li>\n<li>Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.</li>\n<li>Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.</li>\n<li>Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.</li>\n<li>Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.</li>\n<li>Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.</li>\n<li>Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.</li>\n<li>Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.</li>\n<li>Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or health-related field (or equivalent experience).</li>\n<li>Requires at least 1 year of on-site monitoring experience.</li>\n<li>Strong understanding of GCP, ICH guidelines, and regulatory requirements.</li>\n<li>Ability to travel as required by the project.</li>\n</ul>\n<p>The potential base pay range for this role, when annualized, is $74,500.00 - 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sofia-Bulgaria/Senior-Site-Contract-Associate---IQVIA-Biotech_R1557731","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sofia-Bulgaria/Senior-Site-Contract-Associate---IQVIA-Biotech_R1557731","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["life sciences","health care","contract negotiation","clinical trial management","GCP/ICH","regulatory guidelines","Microsoft 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Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.</li>\n<li>Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities.</li>\n<li>Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.</li>\n<li>Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.</li>\n<li>Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory.</li>\n<li>Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.</li>\n<li>May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.</li>\n<li>Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.</li>\n<li>Assists with, and attends, Investigator Meetings for assigned studies.</li>\n<li>Attends study-related, company, departmental, and external meetings, as required.</li>\n<li>Ensures all study deliverables are completed per IQVIA Biotech and study timelines</li>\n<li>Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.</li>\n<li>Serves as mentor for junior CRAs and those new to the company and/or study.</li>\n</ul>\n<p><strong>KNOWLEDGE, SKILLS AND ABILITIES:</strong></p>\n<ul>\n<li>Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.</li>\n<li>Minimum of 1-2 years of onsite monitoring experience is a must.</li>\n<li>Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.</li>\n<li>Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.</li>\n<li>Able to handle several priorities within multiple, complex trials.</li>\n<li>Able to reason independently and recommend specific solutions in clinical settings.</li>\n<li>Able to work independently, prioritize, and work within a matrix team environment.</li>\n<li>Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.</li>\n<li>Candidates must have strong communication levels of Dutch and English.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Experienced-Clinical-Research-Associate---IQVIA-Biotech_R1522187","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Experienced-Clinical-Research-Associate---IQVIA-Biotech_R1522187","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical research","Good Clinical Practices","GCP/ICH 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compliance with study protocols, regulatory requirements, and sponsor expectations.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Conduct all types of site visits,selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.</li>\n<li>Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.</li>\n<li>Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.</li>\n<li>Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.</li>\n<li>Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.</li>\n<li>Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.</li>\n<li>Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.</li>\n<li>Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.</li>\n<li>Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or health-related field (or equivalent experience).</li>\n<li>Requires at least 1 year of on-site monitoring experience.</li>\n<li>Strong understanding of GCP, ICH guidelines, and regulatory requirements.</li>\n<li>Ability to travel as required by the project.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/CRA-2--Argentina--IQVIA-Biotech_R1540400","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/CRA-2--Argentina--IQVIA-Biotech_R1540400","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","ICH guidelines","regulatory requirements","life sciences","health-related 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support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.</li>\n<li>Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.</li>\n<li>Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.</li>\n<li>Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.</li>\n<li>Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts, managers and directors as required.</li>\n<li>Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.</li>\n</ul>\n<p><strong>Qualifications and Skills</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in life sciences or health care</li>\n<li>+6 years relevant experience, including demonstrable experience acting as a contract negotiator.</li>\n<li>Relevant sponsor or clinical research organization clinical site contracting experience.</li>\n<li>Good negotiating and communication skills.</li>\n<li>Good interpersonal skills and a strong team player.</li>\n<li>Strong technical writing skills.</li>\n<li>Understanding of regulated clinical trial environment and knowledge of drug development process.</li>\n<li>Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.</li>\n<li>Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.</li>\n<li>Good organizational and planning skills.</li>\n<li>Strong knowledge of Microsoft Office and e-mail applications.</li>\n<li>Ability to interpret pricing models and to prepare proposals, bid grids and budgets.</li>\n<li>Good understanding of clinical trial contract management.</li>\n<li>Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Paris-France/Senior-Site-Contract-Associate---IQVIA-Biotech_R1557455","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Paris-France/Senior-Site-Contract-Associate---IQVIA-Biotech_R1557455","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["life sciences","health care","contract negotiation","clinical trial contract management","GCP/ICH","Microsoft Office"],"x-skills-preferred":[],"x-benefits":["equity"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-05T00:00:00.000Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"life sciences, health care, contract negotiation, clinical trial contract management, GCP/ICH, Microsoft Office"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_2f19cf1a-53f"},"title":"Sr. Site Contracts Associate","description":"<p>IQVIA Biotech is seeking a Sr. Site Contracts Associate with 3-5 years of experience in negotiating clinical site contracts and budget templates. As a Sr. Site Contracts Associate, you will develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs.</p>\n<p><strong>Essential Functions:</strong></p>\n<ul>\n<li>Develop and coordinate investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process.</li>\n<li>Create contract language, payment language, and budget templates as required.</li>\n<li>Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs.</li>\n<li>Ensure collaboration with sponsors, stakeholders, and RSU regions and countries to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.</li>\n<li>Provide specialist legal, operational, and financial contracting support to the Study Teams.</li>\n<li>Assist with 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Plan"],"x-benefits":["equity"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T23:30:16.302Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Buenos Aires"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial contract management, GCP/ICH, regulatory guidelines, negotiation, communication, legal writing, financial writing, technical writing, Grant Plan"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ff3bdb69-087"},"title":"Sr. Site Contracts Associate","description":"<p>IQVIA Biotech is seeking a Sr. Site Contracts Associate in Brazil with 5 years of experience in negotiating clinical site contracts and budget templates.</p>\n<p>The successful candidate will develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Developing and coordinating investigator grants and estimates, contracting strategies, and proposal text</li>\n<li>Creating contract language, payment language, and budget templates</li>\n<li>Utilizing and maintaining contracting systems, tools, processes, and training materials</li>\n<li>Collaborating with sponsors, stakeholders, and RSU regions and countries</li>\n<li>Providing specialist legal, operational, and financial contracting support</li>\n<li>Assisting with the creation and review of core scientific, technical, and administrative documentation</li>\n<li>Contributing to the collection, interpretation, analysis, and dissemination of accurate contracting intelligence</li>\n<li>Ensuring overall contracting efficiency and adherence to project timelines and financial goals</li>\n<li>Reporting contracting performance metrics and out of scope contracting activities</li>\n<li>Working with Quality Management to ensure appropriate contract management and quality standards</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field</li>\n<li>3-5 years of relevant sponsor or clinical research organization clinical site contracting experience</li>\n<li>Good negotiating and communication skills</li>\n<li>Strong legal, financial, and/or technical writing skills</li>\n<li>Strong understanding of regulated clinical trial environment and knowledge of drug development process</li>\n<li>Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-Site-Contracts-Associate--IQVIA-Biotech_R1522475","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-Site-Contracts-Associate--IQVIA-Biotech_R1522475","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial contract management","GCP/ICH","regulatory guidelines","negotiation","communication","legal writing","financial writing","technical writing"],"x-skills-preferred":[],"x-benefits":["equity"],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T23:30:09.337Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"São Paulo"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial contract management, GCP/ICH, regulatory guidelines, negotiation, communication, legal writing, financial writing, technical writing"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c606fde9-828"},"title":"Sr. Site Contracts Associate","description":"<p>IQVIA Biotech is hiring a Sr. Site Contracts Associate in Mexico to develop and implement global contracting strategies for selected sponsors, studies, or multi-protocol programs.</p>\n<p>The successful candidate will 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standards</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree in a related field</li>\n<li>3-5 years of relevant sponsor or clinical research organization clinical site contracting experience</li>\n<li>Good negotiating and communication skills</li>\n<li>Strong legal, financial, and technical writing skills</li>\n<li>Understanding of the regulated clinical trial environment and drug development process</li>\n<li>Knowledge of GCP/ICH and applicable regulatory guidelines</li>\n<li>Ability to develop and suggest alternate contracting language, terms, and financial options</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Mexico-City-Mexico/Senior-Site-Contracts-Associate_R1548202","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA 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guidelines, negotiating, communication, legal writing, financial writing, technical writing"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_a9d8733d-69a"},"title":"Senior Clinical Trial Manager","description":"<p>IQVIA Biotech is seeking a Senior Clinical Trial Manager with oncology experience and a global perspective.</p>\n<p>As a key member of the project team, the Clinical Trial Manager is responsible for conducting clinical studies to meet contractual requirements, in accordance with Standard Operating Procedures (SOPs), policies, and best practices.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Ensure the execution of clinical trials for assigned projects, in accordance with regulatory requirements, client requirements, and internal requirements.</li>\n<li>Ensure that project recruitment targets are met and implement appropriate recruitment strategies.</li>\n<li>Contribute to the development of the project risk management plan and manage clinical risks throughout its lifecycle.</li>\n<li>Ensure the quality of clinical trials by identifying quality standards and requirements, planning compliance assessment methods, and monitoring and managing clinical quality issues.</li>\n<li>Manage the clinical aspects of project funding, including the Estimate at Completion (EAC).</li>\n<li>Identify and manage the project&#39;s clinical stakeholders, both internal and external, through effective communication and rigorous issue management.</li>\n<li>Collaborate with the clinical team to achieve established objectives.</li>\n<li>Plan the clinical team&#39;s resources and talent.</li>\n<li>Lead regular team meetings and communicate effectively to achieve objectives.</li>\n<li>Contribute to professional development by providing feedback to the clinical team&#39;s frontline managers on their performance against project tasks.</li>\n<li>Participate, as appropriate, in the development of the clinical delivery strategy for proposals.</li>\n<li>May mentor and train new colleagues during their onboarding.</li>\n<li>May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.</li>\n<li>May participate in site visits, as required, to support project execution.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in health sciences or another scientific discipline required.</li>\n<li>5 years of experience in clinical research/monitoring or an equivalent combination of education and experience required.</li>\n<li>Basic knowledge of project management practices and terminology required.</li>\n<li>Sound knowledge of regulatory requirements applicable to clinical research, including Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.</li>\n<li>In-depth knowledge of protocols and therapeutic aspects.</li>\n<li>Understanding of the financial aspects of projects.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive salary</li>\n<li>Opportunity to work with a leading global provider of clinical research services, commercial insights, and healthcare intelligence</li>\n<li>Collaborative and dynamic work environment</li>\n</ul>\n<p><strong>About IQVIA:</strong></p>\n<p>IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Chef-principal-des-essais-cliniques--IQVIA-Biotech-Senior-Clinical-Trial-Manager--IQVIA-Biotech_R1530647","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Chef-principal-des-essais-cliniques--IQVIA-Biotech-Senior-Clinical-Trial-Manager--IQVIA-Biotech_R1530647","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","International Conference on Harmonisation (ICH) guidelines","project management","clinical research","monitoring"],"x-skills-preferred":["oncology experience","global perspective"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T22:12:58.379Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, project management, clinical research, monitoring, oncology experience, global perspective"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_dccaaaa6-7b8"},"title":"Sr. CRA 1","description":"<p>IQVIA Biotech is seeking a Senior Clinical Research Associate (CRA) to work in Brazil, preferably with oncology experience.</p>\n<p>As a 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verifying that the Investigator&#39;s Site File (ISF) is maintained according to GCP and local regulations</li>\n<li>Creating and maintaining documentation regarding site management, monitoring visit findings, and action plans</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific discipline or healthcare (preferred)</li>\n<li>At least 3-4 years of on-site monitoring experience</li>\n<li>Equivalent combinations of education, training, and experience may be considered</li>\n<li>Good knowledge of and skill in applying applicable clinical research regulatory 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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-CRA-1--Brazil_R1543982","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA 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This role ensures successful site selection, activation, monitoring oversight, and closeout,while balancing speed, quality, and cost. 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leads</li>\n</ul>\n<ul>\n<li><strong>Operational Excellence &amp; Risk Management</strong></li>\n<li>Develop and manage integrated study plans and risk mitigation strategies</li>\n<li>Proactively identify risks and implement corrective/preventative actions</li>\n<li>Monitor study timelines, enrollment trends, and data quality metrics</li>\n<li>Ensure compliance with GCP, SOPs, protocols, and regulatory standards</li>\n</ul>\n<ul>\n<li><strong>Financial &amp; Contract Management</strong></li>\n<li>Manage study financials, including forecasting and revenue acceleration</li>\n<li>Identify and manage out-of-scope work and change orders</li>\n<li>Oversee Billing Unit Reviews (BURs) and expense approvals</li>\n<li>Track performance against budget and Estimate at Completion (EAC)</li>\n</ul>\n<ul>\n<li><strong>Quality &amp; Compliance</strong></li>\n<li>Maintain TMF health and ensure timely document submission</li>\n<li>Develop quality monitoring plans and compliance metrics</li>\n<li>Ensure adherence to study tools, training materials, and processes</li>\n</ul>\n<ul>\n<li><strong>Team Leadership &amp; Development</strong></li>\n<li>Lead and mentor cross-functional project teams</li>\n<li>Support CRA and team training on therapeutic areas and study-specific needs</li>\n<li>Foster collaboration, knowledge sharing, and continuous improvement</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li><strong>Required</strong></li>\n<li>Bachelor’s degree in life sciences or related field</li>\n<li>5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role</li>\n<li>Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes</li>\n<li>Experience managing global clinical trials and multi-regional teams</li>\n<li>Demonstrated experience in project financial management</li>\n</ul>\n<ul>\n<li><strong>Core Competencies</strong></li>\n<li>Exceptional communication and stakeholder management skills</li>\n<li>Strong 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guidance.</li>\n<li>Present to clients and professional bodies as needed.</li>\n<li>Maintain accurate internal system documentation, including CTMS, trackers, and project plans.</li>\n<li>Build and maintain strong relationships with preferred clients, serving as liaison for key accounts when required.</li>\n</ul>\n<p>Qualifications &amp; Experience:</p>\n<ul>\n<li>Bachelor’s degree in a related field (required).</li>\n<li>5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert.</li>\n<li>Equivalent combinations of education, training, and experience will be considered.</li>\n<li>Strong negotiation and communication skills, with the ability to challenge and influence.</li>\n<li>Excellent interpersonal skills and proven success working within matrix teams.</li>\n<li>Advanced legal, financial, and technical writing abilities.</li>\n<li>Solid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process.</li>\n<li>Knowledge of local and global regulatory requirements, SOPs, and corporate standards.</li>\n<li>Ability to exercise independent judgment and take calculated risks.</li>\n<li>Strong project leadership skills and experience mentoring others.</li>\n<li>Excellent planning, organizational, and presentation skills.</li>\n<li>Strong proficiency in Microsoft Word, Excel, and other Office tools.</li>\n<li>Deep knowledge of clinical trial contract management processes.</li>\n<li>Proven experience leveraging metrics to establish timelines and deliverables.</li>\n<li>Ability to initiate and grow programs across departments to drive organizational impact.</li>\n</ul>\n<p>What We Offer:</p>\n<ul>\n<li>Opportunity to work on global, high-complexity clinical programs.</li>\n<li>A collaborative, supportive, and growth-oriented environment.</li>\n<li>The chance to influence key clients and shape contracting strategy at scale.</li>\n<li>Career progression and professional development opportunities.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Milan-Italy/Senior-Site-Contracts-Associate--IQVIA-Biotech---Italy_R1566234","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Milan-Italy/Senior-Site-Contracts-Associate--IQVIA-Biotech---Italy_R1566234","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":null,"x-salary-range":"€41,000.00 - €79,800.00","x-skills-required":["clinical trial contracting","contract management","regulatory requirements","GCP/ICH","Microsoft 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In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Conduct all types of site visits,selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.</li>\n<li>Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.</li>\n<li>Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.</li>\n<li>Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.</li>\n<li>Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.</li>\n<li>Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.</li>\n<li>Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.</li>\n<li>Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.</li>\n<li>Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in life sciences or health-related field (or equivalent experience).</li>\n<li>Requires at least 1 year of on-site monitoring experience.</li>\n<li>Strong understanding of GCP, ICH guidelines, and regulatory requirements.</li>\n<li>Ability to travel as required by the project.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Research-Associate--IQVIA-Biotech_R1520473","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Research-Associate--IQVIA-Biotech_R1520473","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","ICH guidelines","regulatory requirements","life sciences","health-related field"],"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":"2026-10-27T13:14:03.020Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"São Paulo"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), ICH guidelines, regulatory requirements, life sciences, health-related field"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9ed23aef-342"},"title":"Oncology & Global Experience Clinical Leads","description":"<p>IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. Agile structure, collaborative culture, and deep therapeutic expertise allow IQVIA to deliver tailored solutions that help bring innovative treatments to patients faster.</p>\n<p>Oncology &amp; Global Experience Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&#39; lives by bringing new drugs to the market faster. The Clinical Lead is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices.</p>\n<p><strong>Essential Functions</strong></p>\n<ul>\n<li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li>\n<li>Accountable for meeting projects&#39; recruitment targets and ensuring appropriate recruitment strategies are in place.</li>\n<li>Contribute to the development of the project risk mitigation plan and manage clinical risks through the project&#39;s lifecycle.</li>\n<li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li>\n<li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC).</li>\n<li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li>\n<li>Collaborate with the clinical team to support milestone achievements.</li>\n<li>Resourcing and Talent Planning of the clinical team.</li>\n<li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li>\n<li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li>\n<li>May contribute to the development of the clinical delivery strategy for proposals.</li>\n<li>May mentor and coach new peers as they assimilate into this role.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree in health care or other scientific discipline required.</li>\n<li>Requires 5 years clinical research/monitoring experience or equivalent combination of education, training and experience.</li>\n<li>Requires basic knowledge of Project management practices and terminology.</li>\n<li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li>\n<li>Requires broad protocol knowledge and therapeutic knowledge.</li>\n<li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li>\n<li>Requires understanding of project finances.</li>\n<li>Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.</li>\n<li>Communication - Strong written and verbal communication skills including good command of English language.</li>\n<li>Problem solving - Problem solving skills.</li>\n<li>Organization - Planning, time management and prioritization skills.</li>\n<li>Prioritization - Ability to handle conflicting priorities.</li>\n<li>Quality - Attention to detail and accuracy in work.</li>\n<li>Leadership - Good influencing and negotiation skills.</li>\n<li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.</li>\n<li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li>\n<li>Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Trial-Manager-II--IQVIA-Biotech_R1520718","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Trial-Manager-II--IQVIA-Biotech_R1520718","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","International Conference on Harmonization (ICH)","Project management","Clinical trials","Communication","Problem solving","Organization","Leadership","Microsoft Office"],"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":"2026-10-21T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"São Paulo"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), International Conference on Harmonization (ICH), Project management, Clinical trials, Communication, Problem solving, Organization, Leadership, Microsoft Office"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_7b2c0a43-9c3"},"title":"Senior Clinical Research Associate (Sr CRA 3)","description":"<p>IQVIA Biotech is seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Brazil.</p>\n<p>In this role, you will independently manage and monitor clinical trial sites to ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, regulatory requirements, and sponsor expectations.</p>\n<p>As a key member of the study team, you will perform site monitoring activities including site qualification, initiation, routine monitoring, and closeout visits. You will partner closely with investigative sites to support patient recruitment and retention efforts, provide protocol and study-related training, and proactively identify and resolve quality or compliance issues.</p>\n<p>The Sr CRA 3 is responsible for overseeing site performance, tracking study milestones, reviewing source documentation, managing data query resolution, ensuring regulatory and essential documents are maintained, and documenting monitoring activities through timely and accurate reports. You will collaborate with cross-functional teams to support the successful execution of clinical trials and may mentor junior CRAs through co-monitoring and training activities.</p>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree in a scientific, healthcare, or related discipline (or equivalent combination of education and experience).</li>\n<li>Minimum of 4 years of on-site clinical monitoring experience.</li>\n<li>Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes.</li>\n<li>Experience conducting monitoring visits across multiple phases of clinical research.</li>\n<li>Excellent organizational, communication, and problem-solving skills.</li>\n<li>Ability to effectively manage multiple priorities in a fast-paced environment.</li>\n<li>Proficiency with Microsoft Office applications and clinical trial systems.</li>\n</ul>\n<p><strong>Preferred Skills</strong></p>\n<ul>\n<li>Strong therapeutic area knowledge and protocol management experience.</li>\n<li>Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams.</li>\n<li>Experience mentoring or supporting the development of junior clinical research professionals.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-CRA-3--Brazil--IQVIA-Biotech_R1559482-4","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-CRA-3--Brazil--IQVIA-Biotech_R1559482-4","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","ICH guidelines","FDA regulations","clinical trial 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engagement","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":93100,"maxValue":232800,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_81668a3d-c25"},"title":"Clinical Trial Manager II","description":"<p>IQVIA Biotech is seeking a Clinical Trial Manager with oncology experience and a global perspective.</p>\n<p>As a Clinical Trial Manager, you will play a vital role in the conduct of clinical trials. You will work closely with clinical teams to contribute to improving patients&#39; lives by accelerating the commercialization of new medicines.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Ensure the execution of clinical trials for assigned projects, in accordance with regulatory requirements, client requirements, and internal requirements.</li>\n<li>Identify and manage project clinical stakeholders, both internal and external, through effective communication and rigorous issue management.</li>\n<li>Collaborate with the clinical team to achieve established objectives and report to internal and external stakeholders as required by the project.</li>\n<li>Plan the clinical team&#39;s resources and talent, and coach the clinical team at the project level to ensure its success.</li>\n<li>Lead regular team meetings and communicate effectively to achieve objectives.</li>\n<li>Contribute to professional development by providing feedback to the clinical team&#39;s frontline managers on their performance against project tasks.</li>\n<li>Participate in the development of the clinical delivery strategy for proposals and develop and present the clinical operations plan.</li>\n<li>May mentor and train new colleagues during their onboarding.</li>\n<li>May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.</li>\n<li>May participate in site visits, as required, to support project execution.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in health sciences or another scientific discipline required.</li>\n<li>5 years of experience in clinical research/monitoring or an equivalent combination of education and experience required.</li>\n<li>Basic knowledge of project management practices and terminology required.</li>\n<li>Sound knowledge of regulatory requirements applicable to clinical research, including Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.</li>\n<li>In-depth knowledge of protocols and therapeutic aspects.</li>\n<li>Understanding of the financial aspects of projects.</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive salary</li>\n<li>Opportunity to work with a leading global provider of clinical research services, commercial insights, and healthcare intelligence</li>\n<li>Collaborative and dynamic work environment</li>\n</ul>\n<p>IQVIA is an equal opportunity employer and welcomes applications from all qualified candidates.</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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Gestionnaire-d-essais-cliniques-II-CTM-II--IQVIA-Biotech_R1571601","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Gestionnaire-d-essais-cliniques-II-CTM-II--IQVIA-Biotech_R1571601","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","International Conference on Harmonisation (ICH) guidelines","project management","clinical research","monitoring"],"x-skills-preferred":["oncology experience","global perspective"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-26T01:51:12.197Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kirkland, Quebec"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, project management, clinical research, monitoring, oncology experience, global perspective"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b33a2a72-385"},"title":"CTM II or Senior CTM","description":"<p>Join IQVIA Biotech as a Senior Clinical Lead and take the lead on complex, global clinical trials to help bring innovative therapies to patients faster. You will drive clinical strategy, lead international study teams, and play a critical role in delivering world-class research programs.</p>\n<p><strong>What You&#39;ll Do</strong> As a Senior Clinical Lead, you will provide leadership and oversight for large, multi-regional clinical trials, ensuring studies are delivered on time, within scope, and to the highest quality standards. You&#39;ll partner with cross-functional teams, sponsors, and stakeholders to navigate challenges, drive recruitment success, manage risk, and achieve key project milestones.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Lead the clinical delivery of large global clinical trials from startup through closeout.</li>\n<li>Drive patient recruitment and retention strategies to meet enrollment goals.</li>\n<li>Identify, assess, and mitigate clinical and operational risks.</li>\n<li>Oversee clinical quality, ensuring compliance with ICH-GCP, regulatory requirements, and study protocols.</li>\n<li>Partner with project leadership to manage timelines, budgets, and resource planning.</li>\n<li>Build, mentor, and guide clinical teams to deliver exceptional results.</li>\n<li>Collaborate with internal and external stakeholders across multiple regions and cultures.</li>\n<li>Support proposal development, bid defenses, and strategic planning activities.</li>\n</ul>\n<p><strong>What We&#39;re Looking For</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific, healthcare, or related field.</li>\n<li>Sr CTM Requirements: 7+ years of clinical research experience, including monitoring and clinical trial leadership.</li>\n<li>CTM II Requirements: 5+ years of clinical research experience, including monitoring and clinical trial leadership.</li>\n<li>Strong knowledge of clinical operations, ICH-GCP guidelines, and global regulatory requirements.</li>\n<li>Experience leading complex, multi-country studies and cross-functional teams.</li>\n<li>Understanding of project management principles and clinical trial financial oversight.</li>\n<li>Excellent communication, stakeholder management, and problem-solving skills.</li>\n<li>Proven ability to influence, mentor, and drive results in a fast-paced environment.</li>\n</ul>\n<p><strong>Why Join Us?</strong></p>\n<ul>\n<li>Lead high-impact global clinical programs</li>\n<li>Collaborate with industry-leading experts and sponsors</li>\n<li>Influence strategy and operational excellence across studies</li>\n<li>Mentor and develop talented clinical professionals</li>\n<li>Help advance innovative treatments that improve patient 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://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/XMLNAME--Senior--Clinical-Trial-Manager--II---IQVIA-Biotech_R1571600","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/XMLNAME--Senior--Clinical-Trial-Manager--II---IQVIA-Biotech_R1571600","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$93,100.00 - $232,800.00","x-skills-required":["clinical research","ICH-GCP guidelines","global regulatory requirements","project management","clinical trial financial oversight","communication","stakeholder management","problem-solving"],"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":"2026-10-26T01:51:11.645Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical research, ICH-GCP guidelines, global regulatory requirements, project management, clinical trial financial oversight, communication, stakeholder management, problem-solving","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":93100,"maxValue":232800,"unitText":"YEAR"}}}]}