Monitoring Oncology Clinical Trials

Site Data Management

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

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