Responsibilities of this position include the oversight of an NIMH-funded clinical trial investigation from protocol development through manuscript submission to achieve study objectives. Study oversight includes regulatory, compliance, and research protection procedures including protocol development and correspondence. Responsibilities also include scheduling and overseeing the data safety monitoring board (DSMB), the monitoring and reporting adverse events, and managing unanticipated problems including protocol deviations. Duties include start-up activities, documentation/template development, digital health intervention development and implementation, assessment procedure development and implementation, participant recruitment/enrollment, and oversight of study staff.