Onsite Clinical Monitoring Associate – Interventional Trials

IQVIA UK’s cFSP team is expanding and seeks experienced Clinical Research Associates in the South West England to perform site monitoring visits in line with GCP/ICH guidelines and sponsor requirements. You will coordinate with sites, manage expectations, and support regulatory submissions throughout trials.

Join IQVIA for a mission to accelerate innovation for healthier outcomes, with flexible working, mentorship, and clear career development opportunities offered.

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