Clinical Research Coordinator

Works with and under the direction of the Principal Investigator (PI).  While the PI is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.  By performing these duties, the CRC works with the PI, sponsor, management, and other coordinators to support and provide guidance on the administration of the compliance, financial, personnel, and other related aspects of the clinical study.

The CRC reports primarily to the PI, with associated responsibilities to the Manager.