CLR 430 - Managing and Monitoring Clinical Trials

Credits: 3

Theoretical and practical overview of managing and monitoring clinical trials including roles and responsibilities, protocol implementation, data collection strategies, monitoring investigator data during clinical trials, importance of audits and inspections, detecting fraudulent data, IRB processes at clinical sites, required study documents, subject recruitment, project management and CRO team structures.

Click here for the Spring 2025 Class Schedule.