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.
Successful completion fulfills the study staff GCP training requirement for 3 years.
Every Tuesday, June 6-27, 2023, 8-11:30 am EDT
Session: 3.5 hours