{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/at/icon/"},"x-facet":{"type":"company","slug":"icon","display":"ICON","count":57},"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. 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Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in business administration, facilities management, or a related field preferred.</li>\n<li>Previous experience in facilities management, administrative duties, or related roles is advantageous.</li>\n<li>Strong organizational and time management skills with the ability to prioritize tasks effectively.</li>\n<li>Proficiency in Microsoft Office Suite and familiarity with facility management software is a plus.</li>\n<li>Excellent communication and interpersonal skills with a customer service-oriented approach.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_8393d65b-a4c/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Facilities---Admin-Coordinator_JR158444?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":["Microsoft Office Suite","facility management software","organizational skills","time management skills","communication skills","interpersonal skills"],"x-skills-preferred":["Bachelor's degree in business administration","facilities management experience","administrative duties experience"],"datePosted":"2026-10-26T09:38:56.175Z","occupationalCategory":"Facilities & Maintenance","industry":"Healthcare","skills":"Microsoft Office Suite, facility management software, organizational skills, time management skills, communication skills, interpersonal skills, Bachelor's degree in business administration, facilities management experience, administrative duties experience"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_fd585da4-f3a"},"title":"Clinical Trial Manager","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes. 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Required qualifications and experience:</p>\n<ul>\n<li>University degree in medicine, science, or equivalent combination of education &amp; experience</li>\n<li>Experience in global clinical trial management is required</li>\n<li>Demonstrated ability to drive the clinical deliverables of a study</li>\n<li>Subject matter expertise in the designated therapeutic area</li>\n<li>Prior monitoring experience is preferred</li>\n<li>Willingness to work in a home-based setup</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_fd585da4-f3a/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Philippines-Manila/Clinical-Trial-Manager_JR158418?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial management","global clinical trials","regulatory compliance","risk management"],"x-skills-preferred":["monitoring experience","therapeutic area expertise"],"datePosted":"2026-10-26T09:38:55.619Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial management, global clinical trials, regulatory compliance, risk management, monitoring experience, therapeutic area expertise"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9f9adecd-19d"},"title":"Shipping Coordinator","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. 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Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_f2764276-c45/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Salt-Lake-City-PRA/Medical-Research-Associate--Certified-Phlebotomist-Medical-Assistant-CNA-_JR160790?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":null,"x-job-type":"PRN/As Needed","x-salary-range":null,"x-skills-required":["English","phlebotomy","vital signs assessment"],"x-skills-preferred":["Basic Life Support (BLS)","Phlebotomist Certification","Medical Assistant","Certified Nursing Assistant","Certified Medication Aide","Telemetry Technician","Laboratory Technician"],"datePosted":"2026-10-26T08:55:37.503Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Salt Lake City, UT"}},"occupationalCategory":"Healthcare","industry":"Healthcare","skills":"English, phlebotomy, vital signs assessment, Basic Life Support (BLS), Phlebotomist Certification, Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, Laboratory Technician"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_137dd03e-837"},"title":"Manager, Sales Operations","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>At ICON our Sales Operations team plays a critical role in shaping commercial strategy and driving business growth through data-driven decision making. 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As a Lead Consultant, you will be responsible for managing all aspects of systematic literature reviews and evidence synthesis projects, ensuring high-quality deliverables that meet client requirements.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Managing projects and ensuring quality deliverables</li>\n<li>Establishing and maintaining client relationships and leading proposal development</li>\n<li>Providing oversight of resourcing, staff development, and departmental growth</li>\n<li>Contributing to business development and proposal processes</li>\n<li>Mentoring junior reviewers and providing training and support</li>\n<li>Leading publications and scientific communications</li>\n<li>Directing, managing, and being involved in proposal writing, project work, and client liaison</li>\n<li>Supporting senior leadership in implementing business strategies</li>\n<li>Being part of the management team of the global practice</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Master&#39;s degree or higher in public health, health economics, or a related quantitative discipline</li>\n<li>Experience in designing and leading systematic literature reviews and evidence synthesis</li>\n<li>Significant relevant industry or consultancy experience</li>\n<li>Demonstrable experience of people management and business development</li>\n<li>Proven management experience, particularly in leading a team of junior analysts</li>\n<li>Ability to work effectively as part of a team and high self-motivation</li>\n<li>Leadership potential</li>\n</ul>\n<p>We offer a competitive and comprehensive total rewards package, including:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_ff4c5604-afe/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Lead-Consultant---Systematic-Reviews---Evidence-Synthesis_JR144602?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["systematic literature reviews","evidence synthesis","health economics","epidemiology","people management","business development"],"x-skills-preferred":[],"datePosted":"2026-10-26T08:33:36.826Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Consulting","industry":"Healthcare","skills":"systematic literature reviews, evidence synthesis, health economics, epidemiology, people management, business development"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c776f7c4-6d7"},"title":"Senior Medical Writer","description":"<p>ICON is seeking a Senior Medical Writer to join their team. As a Senior Medical Writer, your primary responsibility will be to provide scientific and medical/clinical writing support as part of a team dedicated to late-phase projects, servicing an assigned client.</p>\n<p>The Role: The primary responsibilities and accountabilities of our Senior Medical Writer are:</p>\n<ul>\n<li>Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.</li>\n<li>Responsible for developing scientific communication such as abstract, poster, manuscript, etc.</li>\n<li>Responsible for performing quality control for medical writing deliverables</li>\n<li>Responsible for interpreting statistical results and for soliciting statistician input for developing study reports, abstracts, manuscripts, and other documents as required</li>\n<li>Participating in the improvement of the quality assurance system</li>\n<li>Responsible for participating in bid-defence presentations representing medical writing activities</li>\n</ul>\n<p>What you need:</p>\n<ul>\n<li>Advanced degree in a scientific discipline, preferably PhD, PharmD or MD</li>\n<li>5+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting</li>\n<li>Proven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry standard</li>\n<li>Outstanding written and verbal interpersonal skills</li>\n<li>Good computer literacy</li>\n<li>Ability to work effectively and cooperatively with cross-functional teams</li>\n</ul>\n<p>Rewards &amp; Benefits: ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_c776f7c4-6d7/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Medical-Writer_JR158235?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":null,"x-salary-range":null,"x-skills-required":["Medical Writing","ICH/GCP","GPP guidelines","Scientific Communication","Statistical Analysis"],"x-skills-preferred":[],"datePosted":"2026-10-26T08:33:31.126Z","jobLocationType":"TELECOMMUTE","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Medical Writing, ICH/GCP, GPP guidelines, Scientific Communication, Statistical Analysis"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1c7c4d51-bc9"},"title":"Site Specialist II","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Site Specialist II, you will support preparation, process and tracking of site level critical documents and/or of site activation tasks required for site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Recognize, exemplify and adhere to ICON’s values of Accountability and Delivery, Collaboration, Partnership and Integrity</li>\n<li>Support Site Partners to collect, review, organize and assemble initial start-up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities</li>\n<li>Support collection and assembling of all documents needed in the Critical Document Package (CDP) and/or those required for site activation</li>\n<li>Perform timely and accurate progress data entry of all documents collected from sites and of the relevant study site activation activities into the appropriate tracking systems and tools</li>\n<li>Participate to internal study review meetings with study teams to provide updates on site progress in document collection and on the executed site activation tasks</li>\n<li>Accurately forecast Site Activation plans and ensure that they are reflected accurately in ICON’s systems</li>\n<li>Ensure accuracy and timely completeness of Trial Master File (TMF) documents submitted during start-up and perform a Quality Control (QC) review of files before transfer to maintenance for filing in TMF</li>\n<li>Attend study team meetings as required</li>\n<li>Other duties as assigned</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in life sciences or a related field</li>\n<li>Very good knowledge of English as well as the local language</li>\n<li>Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities</li>\n<li>Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements</li>\n<li>Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously</li>\n<li>Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_1c7c4d51-bc9/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Georgia-Tbilisi/Site-Specialist-II_JR158149?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"mid","x-job-type":null,"x-salary-range":null,"x-skills-required":["ICH-GCP","regulatory affairs","clinical research","study start-up activities","project management","communication skills"],"x-skills-preferred":[],"datePosted":"2026-10-26T08:33:29.071Z","jobLocationType":"TELECOMMUTE","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"ICH-GCP, regulatory affairs, clinical research, study start-up activities, project management, communication skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ce9f39e7-e61"},"title":"Set Up Specialist","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p>\n<p>We are currently seeking a Set Up Specialist I (SUS) to join our diverse and dynamic team. As a SUS at ICON Central Laboratories (ICL), you will play a pivotal role in setting up the laboratory requirements of clinical trials. You will contribute to the advancement of innovative treatments and therapies by facilitating efficient study setup processes in relation to compliance with study protocols, timelines, operational requirements, and client expectations.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Serve as the primary liaison with the client during the laboratory setup of the study.</li>\n<li>Own the laboratory specifications document completion process. Ensure all information captured in the Laboratory Specifications Document and are accurate by considering the study protocol, client requests, ICL standards, and requests/recommendations from internal operational groups.</li>\n<li>Communicate major decisions or timeline changes during setup with the ICL Project Manager and other ICL staff as necessary (and ICON Clinical CRO if appropriate).</li>\n<li>Work independently to coordinate and manage the completion of the Laboratory Specifications Document, timelines and communication of information as required to the other departments within ICL (and ICON Clinical CRO if applicable).</li>\n<li>Serve as subject matter expert for the client, guiding them through a successful setup process, providing creative solutions by drawing on past experiences and/or ICL standards. Highlight any risks associated with the study to the client and internal parties including participating in internal risk assessment and other operational meetings as necessary.</li>\n<li>Oversee internal database configuration, client approval of site-facing Laboratory Manual and Requisitions based on the Laboratory Specifications Document, and source materials needed for the trial that are required for visit specific kits to sites.</li>\n<li>Present solutions and establish best practices for laboratory setups for new and complex protocol requirements.</li>\n<li>Maintaining accurate records and documentation related to Laboratory Specifications development activities.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Bachelor’s degree in a relevant field such as life sciences, clinical research, or healthcare management.</li>\n<li>Strong understanding of clinical trial processes and laboratory testing.</li>\n<li>Experience interpreting study protocols, regulatory requirements, and GCP guidelines.</li>\n<li>Excellent organizational skills and attention to detail, with the ability to manage multiple setup tasks simultaneously.</li>\n<li>Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.</li>\n<li>Proactive attitude with a willingness to learn and adapt to evolving technologies and processes.</li>\n<li>1+ years of experience working in a clinical trial environment such as project management, site coordination, or database configuration, etc.</li>\n<li>Proficient in Microsoft Office Suite; Word, Excel, PowerPoint</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_ce9f39e7-e61/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Bulgaria-Sofia/Set-Up-Specialist_JR161854?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["life sciences","clinical research","healthcare management","study protocols","regulatory requirements","GCP guidelines","Microsoft Office 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development.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Providing strategic medical leadership and guidance on project teams.</li>\n<li>Offering expert medical and scientific consultation throughout project lifecycles.</li>\n<li>Ensuring compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities.</li>\n<li>Representing the Medical Affairs Department in business development initiatives.</li>\n<li>Providing operational oversight within the Medical Affairs Department as needed.</li>\n</ul>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>Medical degree (MD or equivalent) with specialization in Gastroenterology</li>\n<li>Proven track record of medical leadership and consultation within pharmaceutical or biotechnology industries.</li>\n<li>Strong understanding of regulatory requirements and ethical standards in clinical research.</li>\n<li>Advanced English level, excellent communication and interpersonal skills, with the ability to 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English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e28472e4-626"},"title":"Senior CRA / CRA II","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior CRA / CRA II, you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Monitor the progress of clinical studies and ensure compliance with regulatory requirements</li>\n<li>Conduct site visits and remote monitoring to ensure data quality and study integrity</li>\n<li>Collaborate with cross-functional teams to resolve issues and implement 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assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_b8eead06-58a/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/Clinical-System-Lead_JR161793?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["computer science","software engineering","project management","clinical trial management","data analysis","system integration","data management"],"x-skills-preferred":["Medidata Rave","Veeva"],"datePosted":"2026-10-26T06:48:26.982Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bangalore"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"computer science, software engineering, project management, clinical trial management, data analysis, system integration, data management, Medidata Rave, Veeva"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_409c9629-56f"},"title":"Medical Research Associate (Phlebotomist/Medical Assistant)","description":"<p>ICON is seeking a Medical Research Associate (Phlebotomist/Medical Assistant) to join their team in San Antonio, TX. The successful candidate will play a crucial role in delivering clinical research operations work to a high standard.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Assist in the planning and execution of clinical trials and research studies, including data collection and management.</li>\n<li>Support the research team with literature reviews, data entry, and analysis to inform study protocols and findings.</li>\n<li>Maintain accurate and organized research documentation, ensuring compliance with regulatory and ethical standards.</li>\n<li>Collaborate with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines.</li>\n<li>Assist with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>High School Diploma or equivalency with medical assistant training/certification or other allied health certification.</li>\n<li>Certified Phlebotomist/Medical Assistant or EMT with 2+ years of experience.</li>\n<li>Strong organizational and time management skills, with attention to detail in data collection and documentation.</li>\n<li>Proficiency with research software and tools for data entry, analysis, and reporting.</li>\n<li>Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_409c9629-56f/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-San-Antonio-TX-78232/Medical-Research-Associate-EMT-Phlebotomist-Medical-Assistant-_JR160313?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"onsite","x-experience-level":null,"x-job-type":"PRN/As Needed","x-salary-range":null,"x-skills-required":["Phlebotomy","Medical Assistance","Clinical Research","Data Analysis","Communication"],"x-skills-preferred":[],"datePosted":"2026-10-26T04:19:06.913Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"San Antonio, TX"}},"occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Phlebotomy, Medical Assistance, Clinical Research, Data Analysis, Communication"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_466172ba-a3a"},"title":"Facilities Director - Global CRU & Laboratory Facilities","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>We are seeking an experienced Facilities Director to lead the global strategy, governance, and performance of facilities supporting our Clinical Research Units (CRUs) and Laboratory operations.</p>\n<p>As the technical authority for critical infrastructure, you will be responsible for establishing engineering standards, driving infrastructure reliability, and ensuring our facilities support safe, compliant, and uninterrupted clinical and laboratory operations worldwide.</p>\n<p>Reporting into senior leadership, you will oversee a global facilities organization, lead asset lifecycle and maintenance strategies, and provide expert guidance on major infrastructure investments, business continuity, and operational risk management.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Develop and implement global engineering and maintenance standards across laboratory and clinical research facilities.</li>\n<li>Drive infrastructure reliability, asset management, and business continuity programs.</li>\n<li>Provide technical leadership for critical systems including HVAC, BMS, emergency power, and mechanical and electrical infrastructure.</li>\n<li>Lead facility compliance, inspection readiness, and support GMP-regulated operations.</li>\n<li>Oversee contractor and vendor performance, facilities governance, and continuous improvement initiatives.</li>\n<li>Manage a global facilities budget of approximately $30M and support strategic capital investment programs.</li>\n<li>Lead and develop a geographically dispersed team, building capability and engineering excellence across the organization.</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>10+ years&#39; 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You&#39;ll play a critical role in ensuring the reliability, compliance, and future readiness of facilities that support life-changing research and clinical operations around the world.</p>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_466172ba-a3a/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Ireland-Dublin/Facilities-Director---Global-CRU---Laboratory-Facilities_JR158915?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$30M","x-skills-required":["engineering","facilities management","HVAC","BMS","electrical infrastructure","mechanical infrastructure"],"x-skills-preferred":["Chartered Engineer","professional certifications"],"datePosted":"2026-10-26T04:15:45.458Z","employmentType":"FULL_TIME","occupationalCategory":"Facilities & Maintenance","industry":"Healthcare","skills":"engineering, facilities management, HVAC, BMS, electrical infrastructure, mechanical infrastructure, Chartered Engineer, professional certifications"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_83a4f9af-3f8"},"title":"Clinical Trial Coordinator - Regulatory/Finance","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Clinical Trial Coordinator - Regulatory/Finance in Montreal, Canada, you will be responsible for trial and site administration, document management, regulatory and site start-up responsibilities, budgeting, agreement and payments, and meeting planning.</p>\n<p><strong>Trial and site administration:</strong></p>\n<ul>\n<li>Track and report on essential documents and safety reports</li>\n<li>Ensure collation and distribution of study tools and documents</li>\n<li>Update clinical trial databases and trackers</li>\n<li>Manage clinical supply and non-clinical supply management in collaboration with other country roles</li>\n<li>Coordinate labeling requirements and translation change requests</li>\n</ul>\n<p><strong>Document management:</strong></p>\n<ul>\n<li>Prepare documents and correspondence</li>\n<li>Collate, distribute, and archive clinical documents</li>\n<li>Assist with eTMF reconciliation</li>\n<li>Update manuals and documents</li>\n<li>Document proper destruction of clinical supplies</li>\n<li>Prepare investigator trial file binders</li>\n<li>Execute eTMF quality control plan</li>\n<li>Obtain translations of documents</li>\n</ul>\n<p><strong>Regulatory &amp; Site Start-Up responsibilities:</strong></p>\n<ul>\n<li>Provide and collect forms and lists for site evaluation, validation, and start-up</li>\n<li>Obtain, track, and update study insurance certificates</li>\n<li>Support preparation of submission packages for IRB/ERC and regulatory agencies</li>\n<li>Publish study results where required by local legislation</li>\n</ul>\n<p><strong>Budgeting, Agreement and Payments:</strong></p>\n<ul>\n<li>Develop country and site budgets</li>\n<li>Track and report on negotiations</li>\n<li>Maintain tracking tools</li>\n<li>Contract development, negotiation, approval, and maintenance</li>\n<li>Update and maintain contract templates</li>\n<li>Payment calculation and execution</li>\n<li>Ensure compliance with financial procedures</li>\n<li>Monitor and track adherence and disclosures</li>\n<li>Budget closeout</li>\n</ul>\n<p><strong>Meeting Planning:</strong></p>\n<ul>\n<li>Organize meetings and create study memos, letters, and protocols</li>\n<li>Support local investigator meetings</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>B.A./B.S. in Life Science or equivalent healthcare experience</li>\n<li>Minimum 1-2 years in clinical research or relevant healthcare experience</li>\n<li>At least 2 years of budget negotiation experience</li>\n<li>Fluent in local languages and business proficient in English</li>\n<li>Bilingual in French</li>\n<li>Good understanding of global and country clinical research guidelines</li>\n<li>Hands-on knowledge of good documentation practices</li>\n<li>Good IT skills, including MS Office and clinical IT applications</li>\n<li>ICH-GCP knowledge</li>\n<li>Effective time management, organizational, and interpersonal skills</li>\n<li>High sense of accountability and urgency</li>\n<li>Ability to work independently and in a matrix multicultural environment</li>\n<li>Proactive attitude to solving problems and proposing solutions</li>\n<li>Eligible to work in Canada without visa sponsorship</li>\n</ul>\n<p><strong>Rewards &amp; 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The successful candidate will play a key part in integrating customer identity services into externally facing applications, leveraging Microsoft Entra ID.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Design, implement, and maintain CIAM solutions supporting B2B and B2C identity use cases</li>\n<li>Develop and manage Microsoft Entra ID and Entra External ID / B2C configurations</li>\n<li>Build and maintain identity federation, authentication, and authorization flows</li>\n<li>Integrate CIAM services into externally facing applications and platforms</li>\n<li>Lead or contribute to projects involving B2C customer identity integrations, external partner onboarding, and modernization of legacy authentication platforms</li>\n<li>Ensure CIAM solutions align with broader IAM architecture and security policies</li>\n<li>Provide L3 support for CIAM platforms and integrations</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Strong hands-on experience with Microsoft Entra ID and EntraID B2C / Entra External ID</li>\n<li>Experience implementing OAuth2, OpenID Connect, and SAML</li>\n<li>Experience integrating identity solutions into web and mobile applications</li>\n<li>Understanding of token-based authentication and API security concepts</li>\n<li>Practical experience delivering B2B and B2C identity solutions</li>\n</ul>\n<p><strong>Nice to Have:</strong></p>\n<ul>\n<li>Experience working in regulated environments</li>\n<li>Familiarity with secure SDLC and DevSecOps practices</li>\n<li>Experience with API gateways, microservices architectures, or cloud-native application design</li>\n<li>Scripting / automation experience</li>\n</ul>\n<p><strong>What We Offer:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_677c386f-913/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/CIAM-Engineer_JR159607?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Microsoft Entra ID","EntraID B2C","OAuth2","OpenID Connect","SAML","Identity Federation","Single Sign-On"],"x-skills-preferred":["API gateways","microservices architectures","cloud-native application design","scripting","automation"],"datePosted":"2026-10-26T02:31:35.743Z","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Microsoft Entra ID, EntraID B2C, OAuth2, OpenID Connect, SAML, Identity Federation, Single Sign-On, API gateways, microservices architectures, cloud-native application design, scripting, automation"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_fe7ca16c-df5"},"title":"Senior Clinical System Designer","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Clinical System Designer at ICON, you will design and implement advanced clinical systems that enhance trial design and execution.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs.</li>\n<li>Consolidating and completing high-level system requirements documents and managing their review.</li>\n<li>Copying and modifying CRFs from standard libraries and other studies.</li>\n<li>Providing support and review for the re-use of library items.</li>\n<li>Developing custom CRF screens, edit check and dynamic check specification documents using prototyping methodologies as needed.</li>\n<li>Performing quality control peer reviews of database-related specifications as needed and recording comments appropriately.</li>\n<li>Leading eCRF and other specification review meetings.</li>\n<li>Utilizing edit checks from the appropriate library and modifying them to meet trial-specific requirements.</li>\n<li>Programming more complex dynamic checks and discrepancy edit checks to meet trial-specific requirements.</li>\n<li>Reviewing all activity on an ongoing basis to identify out-of-scope tasks and bringing them to the attention of the CSL.</li>\n<li>Supporting the CSL in negotiating timelines and making decisions on the study.</li>\n<li>Assisting in assessing impacts of post-production database-related changes and compiling change management documentation for review by project team leads.</li>\n<li>Driving post-production database changes and releasing them into production.</li>\n<li>Traveling approximately 10% domestically and/or internationally.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>3+ years of experience in designing and implementing clinical systems within the clinical research industry.</li>\n<li>Expertise in data analysis and interpretation or database development, with proficiency in clinical data management systems and software.</li>\n<li>Knowledge of at least one Clinical Data Management System (e.g., Medidata Rave, Veeva EDC).</li>\n<li>Excellent functional knowledge of Clinical Data Management CRF design tools and ability to plan and design CDMS components directly from interpreting medium-complexity clinical trial protocols.</li>\n<li>Excellent written and verbal communication skills.</li>\n<li>Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above.</li>\n<li>All employees must read, write, and speak fluent English and the host country language.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job 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English, Spanish"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_340ab4a7-c14"},"title":"Clinical Research Associate II","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Clinical Research Associate II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 1 year of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Willingness to travel as required.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_340ab4a7-c14/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Poland-Warsaw/Clinical-Research-Associate-II-Senior-Clinical-Research-Associate_JR151393?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial monitoring","data analysis","communication skills","organisational skills"],"x-skills-preferred":[],"datePosted":"2026-10-26T01:57:14.844Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial monitoring, data analysis, communication skills, organisational skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b10d13c2-3f9"},"title":"Senior Manager, Quality Assurance","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Manager, Quality Assurance at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will manage quality assurance and compliance activities across your area, ensuring your team delivers to the highest standards. Key responsibilities include:</p>\n<ul>\n<li>Developing and implementing quality assurance strategies and processes to support clinical trial activities.</li>\n<li>Conducting comprehensive quality assessments and audits to ensure compliance with regulatory standards and guidelines.</li>\n<li>Collaborating with cross-functional teams to identify and address quality issues and implement corrective actions as needed.</li>\n<li>Participating in the review and approval of clinical trial documentation and data to ensure accuracy and completeness.</li>\n<li>Providing leadership and mentorship to quality assurance staff, fostering a culture of excellence and continuous improvement.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have a strong background in quality assurance and compliance, with proven management experience and a commitment to quality delivery. 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additional EU languages are an advantage.</li>\n<li>Ability to interpret complex medical data and apply technical, scientific and clinical knowledge.</li>\n<li>Strong analytical, problem-solving and critical-thinking skills, with a detail-oriented approach to accuracy and compliance.</li>\n<li>Proactive, self-motivated and able to work both independently and collaboratively.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_973a4329-474/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Germany-Frankfurt/Clinical-Trial-Liaison_JR156558?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MD","PharmD","PhD","clinical research","scientific knowledge","medical knowledge","English","German"],"x-skills-preferred":["additional EU languages"],"datePosted":"2026-10-26T00:58:16.709Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"MD, PharmD, PhD, clinical research, scientific knowledge, medical knowledge, English, German, additional EU languages"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_16ad227b-f3d"},"title":"Senior Medical Writer","description":"<p>ICON is seeking a Senior Medical Writer to join their team. As a Senior Medical Writer, your primary responsibility will be to provide scientific and medical/clinical writing support as part of a dedicated team servicing an assigned client.</p>\n<p>The role involves:</p>\n<ul>\n<li>Interpreting clinical data and adapting it to meet project objectives</li>\n<li>Ensuring compliance with medical publications and communications guidelines</li>\n<li>Representing assigned work at internal and external meetings</li>\n<li>Contributing to client publication and communication plans</li>\n<li>Managing medical writing resources, including junior writers</li>\n<li>Collaborating with the Scientific Manager and account managers to ensure project timelines are met</li>\n</ul>\n<p>Requirements include:</p>\n<ul>\n<li>Advanced degree (PhD, PharmD, or MD)</li>\n<li>Prior relevant experience in medical publications or communications</li>\n<li>Minimum 3-5 years of high-level content development experience</li>\n<li>Proficiency with ICMJE and GPP guidelines</li>\n<li>Ability to work efficiently with network directories and databases</li>\n<li>Familiarity with industry standard resources</li>\n<li>Strong command of the English language</li>\n</ul>\n<p>ICON offers a competitive salary and benefits package, including:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_16ad227b-f3d/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Medical-Writer_JR160946?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["medical writing","clinical data interpretation","compliance guidelines","project management","communication plans"],"x-skills-preferred":["resource organizing","mentoring","business development"],"datePosted":"2026-10-26T00:26:01.783Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"medical writing, clinical data interpretation, compliance guidelines, project management, communication plans, resource organizing, mentoring, business development"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_978763c1-a60"},"title":"IHCRA","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include:</p>\n<ul>\n<li>Controlling the contract full details</li>\n<li>Leading the contract negotiation, and managing site payments</li>\n<li>Coordinating the day-to-day operations of clinical studies, including site management, participant recruitment, and data collection</li>\n<li>Ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines throughout the study lifecycle</li>\n<li>Providing training and support to site staff and investigators on study protocols and operational procedures</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Advanced degree in a relevant field such as life sciences, nursing, or healthcare administration</li>\n<li>Extensive experience in clinical study coordination or clinical trial management, preferably within the pharmaceutical or biotechnology industry</li>\n<li>Strong understanding of clinical trial processes, regulatory requirements, and GCP</li>\n<li>Excellent organisational skills and attention to detail, with the ability to manage multiple studies simultaneously</li>\n<li>Strong communication and interpersonal skills, with the ability to work collaboratively with diverse teams and stakeholders</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_978763c1-a60/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/France-Paris/IHCRA_JR160128?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["VeeVa Systems","Ariba","Apex","RGPS","Grant Plan","Good Clinical Practice (GCP)"],"x-skills-preferred":[],"datePosted":"2026-10-25T23:56:45.535Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"VeeVa Systems, Ariba, Apex, RGPS, Grant Plan, Good Clinical Practice (GCP)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_48755c8b-f6e"},"title":"Investigator Contracts Lead / Site Contracts Lead","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Site Contracts Lead at ICON, you will oversee and coordinate the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies or portfolios.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations. 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Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in law, business, life sciences, or a related field, or equivalent experience.</li>\n<li>Strong experience in clinical site contracting or similar contract negotiation roles within CRO, pharma, or healthcare.</li>\n<li>Good understanding of clinical trial agreements, budget structures, and key legal and compliance considerations.</li>\n<li>Excellent negotiation, communication, and problem-solving skills.</li>\n<li>Organised and detail-oriented, with the ability to manage multiple studies and priorities.</li>\n<li>Collaborative mindset with experience guiding or coordinating the work of others.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_48755c8b-f6e/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Canada-Burlington/Investigator-Contracts-Lead---Site-Contracts-Lead_JR159028?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial agreements","budget structures","contract negotiation","problem-solving","communication"],"x-skills-preferred":[],"datePosted":"2026-10-25T23:06:24.182Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial agreements, budget structures, contract negotiation, problem-solving, communication"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bcbd18ea-4f4"},"title":"Senior CRA Phase I Oncology","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. 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Key responsibilities include:</p>\n<ul>\n<li>Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.</li>\n<li>Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration.</li>\n<li>Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track.</li>\n<li>Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organisational objectives.</li>\n<li>Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team. 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As a Clinical Research Associate (CRA) at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Advanced degree in a relevant field such as life sciences, nursing, or medicine.</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong> ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. 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Key responsibilities include:</p>\n<ul>\n<li>Overseeing day-to-day site management activities, ensuring that clinical trial sites comply with study protocols, regulatory requirements, and timelines.</li>\n<li>Collaborating with site staff and cross-functional teams to resolve issues, monitor progress, and ensure timely data collection and reporting.</li>\n<li>Assisting with site initiation, monitoring visits, and close-out activities to ensure the proper execution of clinical trials.</li>\n<li>Providing guidance and mentorship to junior site management staff, fostering collaboration and process improvement.</li>\n<li>Preparing and maintaining site management documentation, including site reports, communications, and updates on site performance.</li>\n</ul>\n<p>You will have a strong foundation in clinical research, with the experience to work independently and guide others. 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Key responsibilities include:</p>\n<ul>\n<li>Leading and overseeing the planning, execution, and management of clinical trials to ensure timely and successful completion.</li>\n<li>Providing strategic direction and guidance to cross-functional teams to optimize trial outcomes and meet project goals.</li>\n<li>Collaborating with key stakeholders to develop and implement innovative clinical trial strategies.</li>\n<li>Ensuring compliance with regulatory requirements and industry standards throughout the clinical trial process.</li>\n<li>Identifying and mitigating risks to ensure the integrity and quality of trial data.</li>\n</ul>\n<p>You will bring significant clinical operations experience, with a track record of building high-performing teams and delivering results. 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additional EU languages are an advantage.</li>\n<li>Ability to interpret complex medical data and apply technical, scientific and clinical knowledge.</li>\n<li>Strong analytical, problem-solving and critical-thinking skills, with a detail-oriented approach to accuracy and compliance.</li>\n<li>Proactive, self-motivated and able to work both independently and collaboratively.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_35f447a8-177/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://iconplc.com/","logo":"https://logos.yubhub.co/iconplc.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/France-Paris/Clinical-Trial-Liaison_JR156554?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MD","PharmD","PhD","clinical research","scientific knowledge","medical knowledge","English","French"],"x-skills-preferred":["additional EU languages"],"datePosted":"2026-10-25T22:56:21.863Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"MD, PharmD, PhD, clinical research, scientific knowledge, medical knowledge, English, French, additional EU languages"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_eece7f72-761"},"title":"Associate Project Manager, Language Services","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. The Language Services team within ICON is seeking highly skilled and experienced COA/eCOA Project Manager/Associate Project Manager to strengthen our services in China.</p>\n<p>As a Project Manager/Associate Project Manager within ICON Language Services, you will be responsible for managing translation projects for clients, starting from initial communication before project launch, including alignment on project scope and costs, through to overall project management, including coordination with internal and external translators, progress management, quality control, and final delivery.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Managing the planning, execution, and delivery of global and local COA/eCOA projects, ensuring alignment with Industry standards &amp; regulatory requirements,</li>\n<li>Managing local COA/eCOA projects for China with a fast turnaround time,</li>\n<li>Collaborating with cross-functional teams in and outside China to secure deliverables,</li>\n<li>Liaise &amp; collaborate with Local client representatives in China to manage expectations &amp; monitor project progress,</li>\n<li>Developing detailed project plans, budgets, and schedules, while monitoring progress to ensure successful COA project outcomes,</li>\n<li>Facilitating communication and stakeholder engagement to promote collaboration and address any project-related challenges.</li>\n<li>Coordinate between team members and clients throughout project execution.</li>\n<li>Select and assign translators and reviewers according to project requirements.</li>\n<li>Conduct final checks of deliverables and coordinate delivery to clients.</li>\n</ul>\n<p><strong>Required knowledge, skills and abilities:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in life science, linguistic project management, or a related field; advanced degree preferred,</li>\n<li>PM position: +5 years of experience in COA/translation/localization project management at a translation company or in a corporate translation department,</li>\n<li>APM position: +2 years of experience in COA/translation/localization project management at a translation company or in a corporate translation department,</li>\n<li>Business level Chinese and English proficiency</li>\n<li>Proficiency in Microsoft Office applications.</li>\n<li>Excellent verbal and written communication skills,</li>\n<li>Strong leadership skills and the ability to effectively manage cross-functional teams in a matrix environment.</li>\n<li>Strong organizational, planning and time management skills with a focus on achieving project goals and timelines, with high quality standards</li>\n<li>Effective communication and interpersonal skills, facilitating collaboration with diverse teams and stakeholders.</li>\n<li>A commitment to maintaining high standards of quality and compliance in all project-related activities.</li>\n<li>Strong technical skills, familiarity with translation management systems and CAT tools,</li>\n<li>Quality oriented and problem-solving abilities</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong> ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_eece7f72-761/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Beijing/Associate-Project-Manager_JR152795?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["COA/eCOA project management","translation management","localization","Chinese","English","Microsoft Office","leadership","communication","project planning","time management","quality control"],"x-skills-preferred":[],"datePosted":"2026-10-25T22:50:33.280Z","employmentType":"FULL_TIME","occupationalCategory":"Operations","industry":"Healthcare","skills":"COA/eCOA project management, translation management, localization, Chinese, English, Microsoft Office, leadership, communication, project planning, time management, quality control"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_89da8344-2c6"},"title":"Senior Clinical Trial Manager - Brazil and/or Mexico - Remote","description":"<p>ICON is seeking a Senior Clinical Trial Manager to join their team. As a Senior Clinical Trial Manager, you will play a crucial role in ensuring the successful delivery of all clinical aspects of studies. Your expertise and leadership will be instrumental in managing the clinical portion of the budget, developing effective monitoring plans, and driving enrollment to meet project objectives.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation.</li>\n<li>Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.</li>\n<li>Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.</li>\n<li>Timely Study Start-Up &amp; Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.</li>\n<li>Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary.</li>\n<li>Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Previous experience in a Clinical Trial Management position (CTM) at a CRO or Pharmaceutical Organization.</li>\n<li>Bachelor&#39;s degree in health, life sciences, or other relevant fields of study.</li>\n<li>Strong previous relevant experience in clinical trial management CRA monitoring.</li>\n<li>Experience in managing complex or global trials is advantageous.</li>\n<li>Experience working in therapeutic areas such as Cardiovascular, Diabetes, and Obesity as a priority.</li>\n<li>Fluency in English (reading, writing, speaking).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_89da8344-2c6/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/Senior-Clinical-Trial-Manager_JR160570?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":null,"x-salary-range":null,"x-skills-required":["Clinical Trial Management","CRA monitoring","Budget Oversight","Study Oversight","Performance Optimization"],"x-skills-preferred":["Managing complex or global trials","Coaching/mentoring other CTMs","Leading a team of CTMs"],"datePosted":"2026-10-25T22:50:33.083Z","jobLocationType":"TELECOMMUTE","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Clinical Trial Management, CRA monitoring, Budget Oversight, Study Oversight, Performance Optimization, Managing complex or global trials, Coaching/mentoring other CTMs, Leading a team of CTMs"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b6d6221b-ddd"},"title":"Senior Tax Accountant","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Tax Accountant at ICON, you will manage complex tax compliance, reporting, and plan activities across multiple jurisdictions. You will help ensure ICON meets its tax obligations while optimising tax efficiency and manage risk.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Preparing and reviewing corporate tax returns, provisions, and related filings for assigned entities in accordance with local laws and regulations.</li>\n<li>Supporting quarterly and annual tax reporting, including tax account reconciliations and effective tax rate analyses.</li>\n<li>Assisting with tax planning initiatives, transfer pricing support, and evaluation of the tax impact of business transactions.</li>\n<li>Liaising with external advisors and tax authorities, supporting audits and responding to tax queries.</li>\n<li>Monitoring changes in tax legislation and assessing potential impacts on ICON&#39;s tax position.</li>\n<li>Contributing to the enhancement of tax processes, controls, and documentation to improve efficiency and compliance.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in accounting, finance, or a related field; professional qualification (e.g., CPA, ACCA, CTA) preferred.</li>\n<li>Significant experience in corporate tax, ideally within a multinational organisation or professional services firm.</li>\n<li>Strong technical knowledge of corporate taxation and tax accounting standards.</li>\n<li>Excellent analytical and problem-solving skills, with strong attention to detail and accuracy.</li>\n<li>Good communication and interpersonal skills, with the ability to work collaboratively with finance and business stakeholders.</li>\n<li>Organised and proactive, with the ability to manage multiple deadlines in a fast-paced environment.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_b6d6221b-ddd/","directApply":true,"hiringOrganization":{"@type":"Organization","name":"ICON","sameAs":"https://icon.com","logo":"https://logos.yubhub.co/icon.com.png"},"x-apply-url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Chennai/Senior-Tax-Accountant_JR157635?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["corporate taxation","tax accounting","analytical skills","problem-solving","communication"],"x-skills-preferred":["CPA","ACCA","CTA"],"datePosted":"2026-10-25T22:50:32.590Z","employmentType":"FULL_TIME","occupationalCategory":"Finance","industry":"Healthcare","skills":"corporate taxation, tax accounting, analytical skills, problem-solving, communication, CPA, ACCA, CTA"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_973ecc50-f31"},"title":"Proposals Development Associate II (Phase II-III) - Remote, US","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Proposals Development Associate II at ICON, you will contribute to the development of client proposals, supporting the success of clinical trial projects, and advancing innovative treatments and therapies in healthcare.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will take responsibility for proposal development deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include:</p>\n<ul>\n<li>Leading the preparation and development of client proposals, including cost estimates, timelines, and scope of work documents.</li>\n<li>Collaborating closely with cross-functional teams, including clinical operations, project management, and finance, to gather necessary information and ensure proposal accuracy and completeness.</li>\n<li>Conducting comprehensive research and analysis to understand client requirements, competitive landscape, and market trends, informing proposal development strategies.</li>\n<li>Managing proposal process workflows, including tracking proposal status, coordinating review cycles, and ensuring adherence to internal processes and timelines.</li>\n<li>Maintaining proposal templates, databases, and other tools to support efficient and effective proposal development and management.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant proposal development experience, along with the following qualifications and skills:</p>\n<ul>\n<li>Bachelor&#39;s degree in life sciences, business administration, or a related field.</li>\n<li>Minimum of 2-3 years of experience in proposal development, clinical research, or related roles within the pharmaceutical, biotechnology, or CRO industry.</li>\n<li>Strong attention to detail and organisational skills, with the ability to manage multiple tasks and deadlines simultaneously.</li>\n<li>Excellent written and verbal communication skills, with the ability to convey complex information in a clear and concise manner.</li>\n<li>Proficiency in Microsoft Office suite (Word, Excel, PowerPoint) and familiarity with proposal management software or CRM systems is a plus.</li>\n<li>Willingness to travel as required (approximately 5%).</li>\n</ul>\n<p><strong>Rewards &amp; 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