Clinical Research Resources Office--CRRO
Presenter: Rana Leed, MPH, Human Research Education Manager, CRRO
Register here before 2 pm, Monday, July 17
"Attendees will review the various types of study documents and best practices for developing and managing them. Using a mix of presentations and live demonstrations, this session will include recommendations for protocols, consents, and various logs and forms. Designed specifically for research staff, all are welcome to attend including investigators. Both in-person and remote participation is available. In-person attendees are recommended to bring a laptop to build their own forms during this session.”
Objectives:
- Identify the types of essential documents for successful study management and execution
- Learn best practices for developing and formatting study documents that can be applied to protocols, consents, and various essential documents including forms and logs
- Demonstrate document management techniques that can lead to successful IRB submissions and study compliance
Session: 2-hours