Mission and Goals
The Participant and Clinical Interactions Program houses two Clinical Research Units, a Clinical Trials Office, the Human Research Protection Program (including the IRB), and the administration of shared services. The program aims to:
- Connect study teams with institutional resources to ensure high-quality and efficient research.
- Provide exceptional facilities and resources to promote rigorous, reproducible, safe, and efficient research.
- Provide education and training to ensure that studies follow principles of Good Clinical Practice.
Leadership
Jamy Ard, MD
Program Leader