Clinical Research Associate, South East EnglandApplylocations: Reading, Berkshire, United Kingdom: London, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 27, 2026 (15 days left to apply)job requisition id: R1550636Join IQVIA on our mission to accelerate innovation for a healthier world!IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England.Why IQVIA?* Career development opportunities to grow as we grow* AI‐powered career advancement through our internal talent marketplace, Career Connections* Mentorship opportunities across the organisation via Employee Resource Groups* Flexible working to assist work–life balance and professional success* Well‐being support covering your physical, mental, and financial healthAwards* 2026 "Glassdoor Best Place to Work in the UK"* #1 in category - 2026 Fortune World’s Most Admired CompaniesTM list (for the FIFTH consecutive year!)* Brandon Hall Excellence Award for Learning & DevelopmentResponsibilities* Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines* Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues* Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase* Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigators Site File (ISF) is maintained in accordance with GCP and local regulatory requirements* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation* Collaborate and liaise with study team members for project execution support as appropriateRequirements* Requires at least 6 months independent on-site monitoring experience of interventional studies* Experience across start-up, enrolment, maintenance, close-out* Digital literacy, including confidence using AI tools in a professional setting* Degree in scientific discipline / health care or equivalent industry experience* Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines* Ability to establish and maintain effective working relationships with coworkers and clients* Full UK right to work required, this position is not eligible for visa sponsorshipApply today and forge a career with greater purpose, make an impact, and never stop learning!
J-18808-Ljbffr