Fundamentals in the Conduct of Clinical Research (for CR Staff), Part 1 of 4

Clinical Research Resource Office

CRRO staff

CR Fundamentals webpage 

"Designed for general study staff, this four-part quarterly series is held on consecutive Tuesdays, usually in March, June, September, and November.  Topics include human research regulations, Good Clinical Practice (GCP) guidance, clinical research (CR) management responsibilities, requisite CR approvals, and best practices related to recruitment, screening, informed consent, and study documentation."

Register for CR Fundamentals here 

Successful completion fulfills the study staff GCP training requirement for 3 years