Clinical Research Committee Coordinator
Job Summary
Supporting the Moffitt Protocol Review and Monitoring System Committees, the full-time remote Clinical Research Committee Coordinator will manage committee functions, serve as a liaison among key stakeholders, and ensure compliance with monitoring policies and procedures.
Key responsibilities:
- Prepare agendas and review materials for committee meetings to ensure compliance with the Data Safety and Monitoring Plan
- Act as a liaison to Committee Chairmen, Program Leaders, Principal Investigators, Regulatory Specialists, and Study Coordinators
- Coordinate overall support and organization for committee functions and responsibilities
Required qualifications:
- Associate's degree or a high school diploma/GED with a minimum of two years' experience in clinical research
- Certification in an area of clinical research may substitute for the educational requirement
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