Under general supervision, responsible for actively facilitating clinical research by administering and monitoring treatment or research protocols. Assists in the determination of guidelines for the collection of clinical data and/or administration of clinical studies. • Screens, recruits and consents study participants. • Verifies eligibility, completes screening procedures, schedules and conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry and maintains study subject data. • Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data. • Ensures compliance with all federal and local regulations. • Monitors close-out of studies and ensures records are retained for appropriate length of time. • Reviews goals and requirements of any new protocols; plans and designs source documentation for protocol; and coordinates study initiation. • Coordinates and manages clinical research projects for Principal Investigator via study protocol including assessment, planning, evaluation and intervention for the well-being of study participants. • Performs all other duties as assigned. Education: Bachelors degree in Nursing is required. • Ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders. • Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner. • Demonstrated ability to monitor important and complex projects concurrently.