Clinical Trials Coordinator: Study Operations & Compliance
Behavioral Health Market Context
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Job Description
involving human subjects. This position plays a critical role in the day-to-day execution of clinical trials, including participant recruitment, data collection, compliance monitoring, and regulatory documentation.
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Qualifications
Benefits
Responsibilities
- •The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical research studies conducted in a hospital setting, ensuring compliance with regulatory requirements and institutional policies
- •The CRC works closely with principal investigators (PIs), research staff, healthcare providers, and study sponsors to support the implementation and management of clinical trials involving human subjects
- •This position plays a critical role in the day-to-day execution of clinical trials, including participant recruitment, data collection, compliance monitoring, and regulatory documentation
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