- Collect patient data from the electronic medical record according to study protocols
- Accurately enter patient data into online research databases
- Perform administrative duties for the MCORRP research group, including:
- Ordering and monitoring supplies
- Completing timekeeping and payroll
- Filing expense reports
- Assisting with meeting planning, scheduling, and coordination
- Assisting with travel coordination
- Support other special projects, as needed
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
Supervision Received: This position receives direct supervision and reports directly to a Clinical Information Analyst Staff Specialist.
Supervision Exercised: None