Senior Clinical Research Associate - EU (Medical Devices) 30 days ago Europe Oversee CRO and vendor activities while directly contributing to study start-up and conduct including site initiation and monitoring visits.Verify accuracy and completeness of clinical data, source documentation, and regulatory files ensuring compliance with GCP, GDPR, and regulations.Identify and resolve discrepancies in study documentation and maintain Trial Master File for audit readiness. Medical Devices GCP Regulatory Compliance View details Similar jobs