Study Coordinator

A Study Coordinator, also known as a Clinical Research Coordinator (CRC), is responsible for managing and coordinating the daily activities of a clinical trial. The Study Coordinator works under the supervision of the Principal Investigator (PI) and is involved in various aspects of the trial, including participant recruitment, informed consent, data collection, scheduling visits, and ensuring compliance with the study protocol and regulatory requirements. The Study Coordinator serves as a liaison between the research team, participants, and sponsors, playing a crucial role in the successful execution of clinical trials.

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