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Research Study Coordinator I- Full time -Research Administration
General Summary
- Under minimal supervision, coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
- Provides technical support to Principal Investigators.
- Duties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study.
- Direct contact with potential and enrolled study participants expected.
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Provides other support as required.
- Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.
- CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.
- Preferred Skills:
- Knowledge of end to end clinical research processes preferred.
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Clinical trial experience required.
- Organization: Henry Ford Medical Group
- Department: Clinical Trials Office Strateg
- Shift: Day Job
- Union Code: Not Applicable
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