Experience as part of a team with all 8 competency domains is expected:
1. Scientific Concepts and Research Design
2. Ethical Participant Safety Considerations
3. Investigational Products Development and Regulation
4. Clinical Study Operations (GCPs)
5. Study and Site Management
6. Data Management and Informatics
7. Leadership and Professionalism
8. Communication and Teamwork
Additional duties include:
- Screening and enrolling patients
- Managing Databases
- Writing and organizing protocols
- Communicating with regulatory authorities
Supervision Received: This position receives direct supervision and reports directly to faculty principal investigator.
Supervision Exercised: None.