UTS - Temporary Study Coordinator at UNC Chapel Hill

The Study Coordinator is responsible for independently coordinating and managing multiple oncology clinical trials throughout the study lifecycle, including activation, enrollment, conduct, monitoring, and closure. This position works closely with Principal Investigators, research staff, sponsors, and clinical teams to ensure studies are conducted in accordance with protocol requirements, Good Clinical Practice (GCP), federal regulations, and institutional policies.

The role requires direct patient interaction and coordination of research activities across UNC Medical Center, UNC-Chapel Hill campus locations, and affiliated clinics.

Essential Responsibilities

Clinical Trial Coordination

• Independently manage multiple oncology clinical trials from startup through study closeout. • Maintain a comprehensive understanding of assigned study protocols and sponsor requirements. • Coordinate study activation, implementation, monitoring, and closure activities. • Participate in site initiation visits, startup meetings, monitoring visits, and closeout visits. • Maintain study documentation and regulatory records. Participant Recruitment and Management • Identify, screen, recruit, and enroll eligible research participants. • Conduct informed consent discussions and document patient participation. • Coordinate and schedule protocol-required study visits. • Provide participant education and study-related support. • Monitor participant safety and communicate study requirements throughout participation. Data Collection and Documentation • Maintain accurate and complete source documentation. • Enter study data into electronic data capture systems and case report forms. • Resolve data queries within established timelines. • Maintain screening logs, enrollment records, and study tracking tools. • Create and review study-specific source documents and data collection materials. • Participate in routine monitoring visits and audits Biospecimen and Laboratory Support • Coordinate collection, processing, storage, and shipment of research specimens. • Maintain specimen accountability and tracking documentation. • Collaborate with investigators and laboratory personnel regarding specimen analysis and study requirements. • Ensure compliance with biohazard handling and shipping procedures. Regulatory Compliance • Ensure compliance with: • Good Clinical Practice (GCP) • FDA and federal research regulations • Institutional Review Board (IRB) requirements • Sponsor requirements • UNC policies and procedures • Report serious adverse events within required timelines. • Assist with protocol deviation reporting and corrective action plans. • Prepare for and support study monitoring visits and audits. Financial and Administrative Responsibilities • Review billing calendars and study-related financial documentation. • Submit participant reimbursement paperwork. • Ensure study visits are linked appropriately within the electronic medical record system. • Track time and effort reporting as required. • Support study-related administrative functions and reporting. Team Collaboration • Serve as a primary contact for assigned clinical trials. • Work collaboratively with investigators, sponsors, research staff, nursing teams, and clinic personnel. • Assist in training and onboarding new staff members. • Support development of investigator-initiated studies and study materials. • Participate in process improvement and quality initiatives.