Participate in planning, implementation, and execution of the conduct of sponsored clinical trials and grant funded research. Coordinate and review research study procedures to ensure receipt, completeness, and accuracy of study data.Coordinate assigned projects with an emphasis on communication with research sponsors, community partners, clinical services, and university administrators, investigators, and research team members.Screen, recruit, and enroll potential research subjects and track participation over time. Conduct and manage study visits. Deliver participant training materials and programs. Conduct participant interviews and measurements.Complete informed consent processes and data collection procedures. Facilitate institutional review board (IRB) applications, submissions, and updates. Assist in preparation of annual reports for federal, state, and local agencies. Inform IRB of amendments to research studies.Process and ship lab specimens collected per protocol and laboratory manual requirements.Perform lab specimen collection - i.e., phlebotomy, urine, etc.- for each clinical trial as required by protocol and laboratory manual.Monitor adherence to procedures/protocols to ensure optimal subject participation rates and accurate data collection and reporting. Ensure completion of contract requirements and project specifications.Help to facilitate project collaborations as assigned.Other related duties as assigned.