Fellow Non - GME

In broad strokes, the role involves: • Facilitating the recruitment of eligible participants and providing comprehensive support throughout their study participation. • Meticulously organizing and managing study information and materials. • Compiling study findings and contributing to the preparation of reports and summaries for broader review. • Ensuring adherence to project timelines, regulatory guidelines, and obtaining all necessary approvals. • Collaborating closely with clinical and research teams, and actively participating in team discussions and strategic planning.