Clinical Research Associate – On-site Monitor

IQVIA UK is seeking experienced Clinical Research Associates to join the cFSP team in the South West England. The role focuses on on-site monitoring, recruitment planning, regulatory compliance, and site training to ensure trial integrity and patient safety.

Candidates should have at least 2 years of independent monitoring experience in interventional studies, with knowledge of GCP/ICH and UK regulatory requirements.

#J-18808-Ljbffr…