Maintaining and revising IRB protocols assisting with research compliance reports and proceduresSubmitting and maintaining contract requests/renewals for consultants, vendors, partnerships, and volunteersCoordinating digital and community-based recruitment efforts for ongoing clinical trialsManagement of purchase requests for study necessities (i.e., participant compensation, materials needed, refunds)Interfacing with research and other investigative staff to maintain effective communication regarding participant scheduling, data management, and quality controlSupervision of staff conducting data entry and other tasksConducting clinical interviews and assessments in both English and SpanishManagement, cleaning, and preparation of data collected via online survey platformsOrganizing and overseeing data collection and study protocolsOther related functions as assigned