Senior CRA – Phase 1 Monitoring (Flexible Work)

IQVIA UK is seeking a Senior Clinical Research Associate with Phase 1 experience to join the cFSP team in London. You will perform site monitoring visits and ensure GCP/ICH compliance while coordinating with sites to support study conduct.

4+ years of on-site monitoring in interventional trials, valid UK right to work, and strong collaboration are essential. IQVIA offers development opportunities and flexible work arrangements to help deliver patient outcomes.

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