IQVIA UK cFSP team is growing and seeking experienced Clinical Research Associates in South West England. The role involves on-site monitoring across the lifecycle of interventional studies, ensuring GCP/ICH compliance, trainee protocol delivery, and strong site collaboration.
Required are at least 2 years of independent on-site monitoring, a degree in a scientific field, and confidence with AI tools. UK right to work is required; visa sponsorship is not available.
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