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The Role of the Clinical Research Coordinator
This course will explore the role of the clinical research coordinator (CRC) in executing a clinical trial and acting as a liaison to the investigator, sponsor, and monitor. The course will introduce key CRC responsibilities at the site, including subject recruitment, informed consent, source document and CRF completion, and test article accountability. The CRC’s role during site visits, including pre-study, initiation, interim and closure, will be examined.
