This program is organized in collaboration with the office of the Associate Dean for Clinical and Translational Research and the Human Research Protection Program/The Institutional Review Board at the American University of Beirut and it introduces participants to the requirements, guidelines and standards for conducting clinical research.
Target Audience
This workshop is mandatory for Research Assistants, Research Coordinators and non-physician Research staff involved in human subject research projects at AUBMC.
Objectives
By the end of this workshop, participants will be able to:
- Complete and submit IRB applications
- Safeguard research subjects’ welfare, rights and safety
- Manage their research project
RAP Team Members
RAP director: Marlene Chakhtoura, MD, MS
RAP coordinator: Sara Khansa, MBA
Contact Information
Ms. Sara Khansa
Telephone: 961 1350000 ext. 5452
2019/ 2020 RAP Calendar
| Workshops 2019/ 2020 |
| Date |
April 9, 2019
|
Portfolio