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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.
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.