The primary goal of the Clinical Research Coordinator is to uphold research integrity, ensure patient safety and maintain adherence to study protocols.
Key responsibilities include:
* Phlebotomy
* EKGs
* Vital signs monitoring
* Collaboration with study monitors for site visits and communication with Institutional Review Boards
The coordinator oversees research staff, delegating tasks, prioritizing duties, recruiting studies, managing batch shipment schedules, maintaining temperature-controlled areas, updating calibration logs and ensuring timely completion of research tasks within agreed Clinical Trial Agreement timelines.
Additional responsibilities include calendar management and data entry queries. The coordinator plays a crucial role in protecting patient rights and well-being, while upholding high standards of professionalism and expertise in clinical trials.