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IQVIA is seeking experienced Clinical Research Associates in the UK to join their dedicated team, focusing on advancing healthcare through cutting-edge clinical trials. The role emphasizes site monitoring, adherence to regulatory standards, and collaboration with study teams. Ideal candidates will possess a life sciences degree and experience in independent on-site monitoring.
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Job Summary
IQVIA is recognized as #1 in its category on the 2025 Fortune World's Most Admired Companies list for the fourth consecutive year.
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out visits in accordance with regulatory requirements.
Candidates will work with sites to adapt, drive, and track subject recruitment plans to enhance predictability.
Matching Summary
Match Score: 75
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IQVIA is seeking experienced Clinical Research Associates in the UK to join their dedicated team, focusing on advancing healthcare through cutting-edge clinical trials. The role emphasizes site monitoring, adherence to regulatory standards, and collaboration with study teams. Ideal candidates will possess a life sciences degree and experience in independent on-site monitoring.
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Skills & Requirements
Must-have
Independent on-site monitoring experience
Good Clinical Practice GCP knowledge
ICH guidelines expertise
Site recruitment plan management
Trial Master File maintenance
Nice-to-have
Flexible to travel to sites
Collaborative team member
Commitment to continuous learning
Key Requirements
Minimum 6 months independent on-site monitoring
Life science degree or equivalent industry experience