Responsibilities Include: Managing multiple clinical trials, screening study patients in EMR, contacting patients to introduce research studies, consenting patients to studies, scheduling patients for study visits, coordinating procedure/implant day activities, seeing study patients in clinic for follow up visits, administering questionnaires and timed walks, performing EKGs, ordering labs and procedures, reviewing EMR records for adverse events, data entry and query resolution in sponsor's electronic data capture (EDC) systems, responding to sponsor emails, scheduling and overseeing monitor visits, investigational device accountability, billing review, updating subject information in the clinical trial management system (CTMS). Your role is crucial in identifying and recruiting patients, ensuring study adherence, and providing educational and emotional support to participants, ultimately contributing to advancements in healthcare.