The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). CRCs are responsible for overseeing the day-to-day operations of clinical trials and studies. They work under clinical research managers and are tasked with administering clinical trials. They attend seminars and events to promote studies, recruit and screen study participants, as well as document and report on the daily operations of a study. Clinical Research Coordinators may work for pharmaceutical companies, hospital research departments, or private businesses. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

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