Clinical Research Coordinator II

Clinical Research Coordinator II Posting Number: req26073 | Department: Orthopedic Surgery | Location: Tucson Campus, 1501 N. Campbell Ave., Tucson, AZ 85719 USA Position Overview The purpose of this position is to coordinate and participate in the conduct and management of complex clinical research studies under the direction of departmental research leadership and Principal Investigators. The role applies knowledge of clinical research principles to support compliance with study protocols, regulatory requirements, and institutional policies. Visa sponsorship is not available for this position. Duties & Responsibilities Coordinate study visits and study procedures; maintain regulatory and study documentation. Create source documents and provide study-specific training in accordance with protocols and Good Clinical Practice guidelines. Perform participant pre-screening, screening, recruitment, enrollment, and informed consent. Conduct study visits and clinical procedures as required by protocol. Maintain accurate source documentation and study records. Develop study-specific tools including source documents, visit checklists, and training materials. Ensure maintenance and organization of regulatory documentation for IRB submissions, continuing reviews, protocol amendments, and reporting requirements. Monitor and report adverse events, serious adverse events, and protocol deviations in accordance with institutional and sponsor requirements. Perform data collection, entry, management, and quality control checks to ensure accuracy and completeness of study data. Resolve data queries and maintain research databases (REDCap or equivalent systems). Work closely with Principal Investigators to coordinate and execute all aspects of multiple clinical trials. Collect, process, and ship biological specimens according to protocol requirements, ensuring proper chain of custody and storage conditions. Maintain study supplies, inventory, and equipment required for research operations. Communicate effectively with study sponsors, IRB, clinical teams, laboratories, and other stakeholders to ensure study compliance and efficiency. Participate in study initiation, monitoring visits, audits, and close-out activities as required. Responsibilities subject to change based on departmental priorities, study requirements, regulatory obligations, and operational needs. Minimum Qualifications Bachelor’s degree or equivalent advanced learning attained through professional level experience. Minimum of 3 years of relevant work experience, or equivalent combination of education and work experience. Preferred Qualifications Research exposure/experience preferred. Benefits Outstanding U of A benefits include health, dental, and vision insurance; life insurance and disability programs; paid vacation, sick leave, and holidays; tuition reduction for the employee and qualified family members; state retirement plan; access to UA recreation and cultural activities; and more. Compensation Salary: $53,039–$66,299 (Full-time). Exempt FLSA. Grade 7. Full benefits eligible. Open Until Filled: Yes. #J-18808-Ljbffr