The Role of the Clinical Research Coordinator

The clinical research coordinator (CRC) has a key role in executing a clinical trial and acting as a liaison to the investigator, sponsor, and monitor. This course will introduce key CRC responsibilities at the site, including subject recruitment, informed consent, source document and case report form (CRF) completion, and test article accountability. Topics in this course include: CRC, Visits Before Study, Visits During & After Study, Recruitment & Retention, Informed Consent, Source Documentation, Case Report Forms, and Essential Documents. After completing this course, learners will be able to identify the CRC’s key roles in research and patient protection from pre-study visits through study completion.

After this course learners will be able to identify the crc’s key roles in research and patient protection from pre-study visits through study completion.