Co-sponsored by the Center for Faculty Excellence (CFE), Lineberger Comprehensive Cancer Center, and NC TraCS, the purpose of the Clinical Trial Investigator Series (CTIS) is to provide education on how to successfully conduct clinical trials of drugs, devices, and to some extent, non-drug intervention trials. The intended audience is faculty, residents, or fellows who are, or aspire to be, clinical trial investigators. The modules will focus on different topics related to investigators’ responsibilities when conducting clinical trials. This module focuses on understanding the types of adverse events or unanticipated problems to report for drug, device, and non-drug intervention trials. **For faculty and postdocs only**

Presenter: Tim Kuhn, Training Coordinator, Office of Human Research Ethics (OHRE)