Clinical Research Coordinator

Job Description
Supports and works closely with the Principal Investigator and Clinical Nurses to administratively coordinate protocol implementation for multiple research studies. CRC conducts day-to day activities of multiple studies with respect to compliance, regulatory, recruitment, study site initiation, monitoring and close out throughout the course of the research trials. The CRC follows protocol, institutional and regulatory requirements to assure accuracy of the study procedures being conducted. The senior coordinator is responsible for managing and monitoring all data collected by the research coordinator prior to submission to the research sponsor or foundation and provides guidance to the Office of Clinical Research on matters regarding human subject’s research protection laws, regulations, policies, procedures and ethical standards.