Administrative Roles of the Clinical Research Coordinator

This course will address the administrative roles and responsibilities of the Clinical Research Coordinator who has been delegated by a principal investigator to coordinate multiple aspects of a clinical trial at an investigative site. The CRC is the individual who oversees completion of the protocol procedures by coordinating both schedules of patients and staff. While this course will be addressing tasks required to fulfill the administrative roles and responsibilities of a designated CRC, the same tasks are required of any clinical trial. Upon completion of this course, you will be able to identify the CRC role throughout a clinical trial, as well as recognize applicable Good Clinical Practice standards.