Responsibilities include coordinating study start up and implementation; overseeing participant recruitment, screening, enrollment, and retention efforts; managing regulatory documentation; monitoring study timelines and deliverables; coordinating data collection activities; maintaining research databases and study records; facilitating communication among investigators, sponsors, and stakeholders; and supporting the preparation of reports, presentations, manuscripts, and grant applications. The position works collaboratively with principal investigators, research faculty, clinical partners, community organizations, regulatory offices, and research participants to ensure studies are conducted in accordance with approved protocols, sponsor requirements, federal regulations, and University policies.