Clinical Trial Site Coordinator Recruit and screen participants, obtain informed consent, and ensure protocol compliance. Collect and document data accurately, maintaining records per GCP standards. Liaise with investigators, sponsors, and study monitors. A Clinical Trial Site Coordinator will be responsible for managing the day-to-day operations of clinical trials at a specific site. Key responsibilities will include recruiting and screening participants, obtaining informed consent, and ensuring compliance with study protocols and regulatory requirements. They will manage patient visits, collect and document data accurately, and maintain proper records in line with Good Clinical Practice (GCP) standards. The coordinator will also liaise with investigators, sponsors, and study monitors, manage study supplies, and ensure the timely and efficient execution of the trial. Additionally, they will play a crucial role in maintaining the safety and well-being of participants while ensuring the integrity of the clinical data collected.
