The Clinical Trial Investigator Series (CTIS) helps investigators understand their responsibilities when conducting clinical trials of drugs, devices, and other types of interventions for which a clinical trial design might be necessary. The series is open to faculty members, residents, clinical fellows, and postdocs who are, or aspire to be, clinical trial investigators. The Protocol Development module focuses on what to include in a clinical trial protocol, and how this is different than an IRB protocol.  **FOR FACULTY AND POSTDOCS ONLY**

Presenter: Leanne Cartee, Director of Protocol Development, Lineberger Cancer Center

Note: All CTIS modules can be accessed through lecture-capture or real-time webinar. You will need to register for each module to access this series through these other means.