Clinical Research Coordinator V

Coordinate activation, implementation, enrollment, accrual, and maintenance of multiple clinical trial protocols under the direction of clinical PIs in the Department of Surgical Oncology. Ensure studies are conducted in compliance with UL IRB, FDA, and OHRP requirements; assist with recruitment, screening and enrollment of eligible participants; develop accurate source materials; ensure compliant data collection, documentation, and reporting in line with site SOPs; maintain accountability logs; and collaborate with the study team, sponsors, monitors, and regulatory entities to support safety, efficiency, and timely completion of studies.