Clinical Research Coordinator I Exempt

Co-sponsoring clinical trials and research studies by coordinating biospecimen collection, maintaining HIPAA-protected databases linking patient information to biospecimens, serving as the study liaison for participants, investigators, and staff, implementing standard operating procedures, ensuring regulatory and protocol compliance, performing patient chart review and data collection, ensuring compliant data entry into registries and research systems, assisting investigators with protocol development and control documents, and managing flexible hours and project-related inquiries while maximizing cost containment and resource use.