Clinical Research Coordinator

The Clinical Research Coordinator (CRC) assists the principal investigator (PI) and sub investigators with all aspects of study implementation. Although the CRC is responsible for coordination of all activities related to clinical trial implementation, the CRC can only perform those procedures for which he/she is qualified by training and/or licensure.

Coordinates all research study activities with the Principal Investigator and has no direct nursing care responsibilities.

· Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements.

· Assess each proposed study protocol

· Facilitate administrative review and approval of proposed studies

· Develop tactical study procedures

· Develop any necessary study documents not provided by sponsor or IRB

· Educate HCA staff regarding research and study protocols

· Screen and recruit patients base...