Administrative Roles of the Clinical Research Coordinator
This course describes the administrative roles and responsibilities of the Clinical Research Coordinator (CRC). The CRC is an individual who coordinates many aspects of a clinical trial at the investigative site. The CRC’s tasks are formally delegated to them by the principal investigator (PI) and frequently involve both clinical duties (within their professional scope of practice) and coordination activities. 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.
Identify the role of a CRC throughout a clinical trial, as well as recognize applicable Good Clinical Practice standards.