Participate in the Site Qualification Visit, Interim Monitoring Visit, Site Initiation Visit, and Close Out Visit, Serve as the main point of contact after the Site Initiation Visit (SIV) for all monitoring activities, Initiate scheduling of participant clinic visits and ongoing study visits, Attend participant visits, as needed to ensure clinical procedures, lab tests, and other protocol-specific activities are completed as outlined in the protocols, Instruct subjects in protocol procedures, medication compliance, concomitant medications, accurate diary maintenance, self-rating scales, and schedule of events, Provide close oversight and review of data collection, data entry as well as protection of data integrity for all studies assigned to the research team, Provide quality control review of subject/patient charts prior to randomization or screen fail to ensure accuracy of status determination, Monitor enrollment and provide enrollment updates for the clinical team and sponsors, Serve as point of contact to clinical research staff, patient navigators, and sponsors for study-specific information, Supervise timely and accurate transcription of information on source documents, paper Case Report Forms (CRFs), and electronic CRFs, Respond to data queries and other requests from data coordinators and study monitors in a timely manner, Provide backup for other Clinical Research Coordinators and Data coordinators, as needed. Supervise research staff and ensure that they are reviewed regularly, remain relevant, and adhere to policy and procedures, Assist Director of Research in developing strategies for recruitment as appropriate to meet or exceed target enrollments, Distribute and coordinate work assignments, Review study protocol with the Research coordinators, data coordinators, and investigators and ensure everyone is aware of their roles and responsibilities, Evaluate staff performance.