Administrative Roles of the Clinical Research Associate
This course examines the administrative roles and responsibilities of the Clinical Research Associate (CRA) during specific on-site monitor visits conducted at the principal investigator location on behalf of a sponsor. Topics in this course include: Roles and Responsibilities, Monitoring Plan, PSSV and SIV, Source Documents, and Monitoring Functions. After completing this course, learners will be able to identify the general roles and responsibilities of a CRA, with recommended monitoring tasks to be completed at specified time intervals of an ongoing study.