The position requires strong interpersonal and communication skills, cultural competence, and the ability to collaborate effectively with investigators, research staff, interdisciplinary teams, and participants from a variety of backgrounds and lived experiences. The CRA will assist with tracking and reporting adverse events and protocol deviations, study activation, regulatory and compliance activities, and adherence to IRB-approved protocols, HIPAA, Good Clinical Practice (GCP), and applicable federal, state, local, and institutional requirements.