Responsible for overall coordination, organization, management, and efficient implementation of clinical trials. Perform study-related procedures in compliance with protocols including but not limited to drug dispensation, compliance and drug accountability, vital signs, physical exams, phlebotomy, EKG, questionnaires, and surveys. Ensure that all protocol deviations, adverse events, and serious adverse events are detected, captured, recorded, followed, and reported to PI, sponsor/IRB in a timely manner.