Clinical Research Coordinator: Patient Care & Protocol Compliance
Behavioral Health Market Context
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Qualifications
- •The ideal candidate will have experience in coordinating studies, a strong understanding of FDA and GCP regulations, and excellent organizational skills
Responsibilities
- •Medix™ is seeking a Study Coordinator in Salt Lake City, Utah, to manage participant recruitment, ensure protocol compliance, and handle data management for clinical studies
- •Responsibilities include recruiting participants, preparing regulatory documentation, and acting as a liaison among stakeholders
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