Join IQVIA on our mission to accelerate innovation for a healthier world!IQVIA UK''s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and in our category on the 2026 Fortune World''s Most Admired Companies list (for the FIFTH consecutive year!).Apply today and forge a career with greater purpose, make an impact, and never stop learning!Essential Functions• 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.• Create and maintain appropriate documentation reg