The Department of Urology is seeking a ClinicalResearchCoordinatorfor University of Pittsburgh and UPMC-sponsored clinical trials. The position is based at the Shadyside campus but will require traveling to Presbyterian/Montefiore, Magee and Mercy. Prior clinicalresearchexperience is required.

Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.

Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.

Coordinate clinicalresearchstudies and drug/device trials across academic and health system settings.Implementresearchprotocols in accordance with GCP and institutional policies.Prepare and submit IRB applications and modifications; track approval status and maintain regulatory documentation.Assist with clinical trial budget negotiation and reconcile payments in collaboration with theresearchfinance office.Screen and assess patients for study eligibility using protocol-specific inclusion and exclusion criteria.Collect patient data from clinical records, imaging, and lab reports; ensure accurate and timely data entry intoresearchdatabases.Monitor study visits and ensure protocol compliance, including adverse event reporting and documentation of protocol deviations.Collaborate with investigators, sponsors, CROs, and internal stakeholders to facilitate study conduct and communication.Assist in the preparation of progress reports, abstracts, and publications as needed.Supervise and train clinicalresearchassistants, students, or trainees working under study protocols.