The Clinical Research Coordinator (CRC) collaborates with investigators, research teams, clinical departments, IRBs, and sponsors to plan, implement, and manage clinical trials and research projects. Responsibilities include participant recruitment, screening, enrollment, conducting protocol-required visits, data collection, and coordinating sponsor monitoring or federal audits. The CRC ensures compliance with federal and state regulations, institutional policies, and maintains accurate documentation, adverse event reporting, and study drug accountability.
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Plusses:
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