St. Petersburg, FL30+ days ago
p>POSITION SUMMARY: The Clinical Research Coordinator is a member of the study team who, under the direction of the Principal Investigator and Director of Research Operations, is responsible for the overall coordination of assigned minimal-risk studies, including regulatory submissions, screening, recruitment, data collection, and data entry to ensure protocol compliance and human subjects protection.
Coordinate the preparation and submission of regulatory documentation to the sponsor and Institutional Review Board (IRB) during all phases of study conduct, including start-up, continuing reviews, changes in research, problem events, and closure, to ensure human subjects' protection and regulatory compliance.