Clinical Research Coordinator - Technician
- Scientific Concepts and Research Design
- Ethical Participant Safety Considerations
- Investigational Products Development and Regulation
- Clinical Study Operations (GCPs)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication and Teamwork
- Associate degree in Health Science or an equivalent combination of related education and experience.
- ONE of the following:
- Minimum 1 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
- An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
- Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
- Training Requirements:
- PEERRS, HIPAA, CITI GCP.
- Gains appropriate training & knowledge of EMR, CTMS, EDC, databases, etc. as assigned.
- Willing to learn and use available technology and systems to accomplish job requirements.
- Understands the disease process per program.
- Attends and participates in all training classes assigned to this level.
- Assists with training activities of staff and others.
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