The data manager provides timely and ongoing management of clinical trials; the data must be organized well, especially for sites involved in multiple studies. Topics include establishing protocol-specific data review & entry guidelines; quality and timely data; completing case report forms (CRFs); remote data entry; electronic CRFs; patient demographic and emergency contact data; patient databases; and data storage, confidentiality, backup, and security. Also covered: transitioning to a career in clinical data management.
Note: Elective for Professional Certificate in Clinical Trials Design and Management.
Other Credit: BRN, BBS: 8 CE hours.
Course Number: FPM-40261 Credit: 2 units