The position will manage multiple concurrent human-subjects research protocols, including participant recruitment, screening, informed consent, study visits, longitudinal follow-up, regulatory documentation, research data systems, and coordination of procedures involving the Center for Clinical and Translational Science (CCTS), imaging, biospecimen collection, and other University research resources. The ideal candidate will exhibit excellent research management and study coordination experience, strong organizational skills, professionalism and empathy in working directly with research participants, the ability to independently problem-solve complex situations, and excellent interpersonal and communication skills.