Independent knowledge, skills, and abilities within 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
Responsibilities:
- Patient enrollment to clinical studies
- Management of Internal Review Board submissions and renewals
- Administration of patient reported outcome surveys
- Data collection for prospective clinical studies
- Data collection for prospectively collected retrospective databases
- Data management including of prospective study data and retrospective databases
- Clinical process mapping
- Intraoperative specimen collection