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Senior Clinical Research Associate (CRA) – UK📍 Reading🕒 Full-time | ✈️ Travel requiredAbout the RoleWe are seeking an experienced Senior Clinical Research Associate (CRA) in the UK to join a sponsor-dedicated clinical trials team. In this role, you will play a critical part in ensuring the successful execution of multiple clinical trials, maintaining high-quality data, and supporting site performance.You will monitor investigative sites, drive recruitment strategies, ensure compliance with GCP and ICH guidelines, and collaborate closely with cross-functional teams to deliver high-quality study outcomes.Key ResponsibilitiesConduct site monitoring visits: selection, initiation, routine monitoring, and close-outSupport sites in implementing and tracking subject recruitment plans to meet project goalsDeliver protocol and study-specific training to site staffEvaluate site compliance and data quality, escalating issues when necessaryTrack study progress: regulatory submissions, subject enrollment, CRF completion, and data query resolutionEnsure TMF and ISF documentation is complete, accurate, and maintained according to GCP and local regulationsPrepare detailed monitoring reports, follow-up letters, and action plansCollaborate with project teams to support overall study execution and timelinesProvide input during start-up phase and ongoing study activities where requiredRequirementsMinimum 18 months of independent on-site monitoring experienceProven experience managing multiple clinical trial protocols across diverse sitesStrong knowledge of Good Clinical Practice (GCP) and ICH guidelinesDegree in Life Sciences or equivalent industry experienceStrong communication and organisational skillsFlexibility and willingness to travel to sitesPrevious experience in oncology, rare disease, or other therapeutic areas is a plusWhy Apply?Work on cutting-edge clinical trials and make a tangible impact on patient careCollaborate with experienced study teams and gain exposure to next-generation clinical developmentAdvance your career in a dynamic, sponsor-dedicated clinical trials environmentAccess to world-class training and professional development opportunities
