This role will be responsible for the maintenance of accurate and organized records, managing data collection, performing data quality checks, addressing data-related issues, developing and implementing research protocols, ensuring compliance with regulations and ethical guidelines, crafting core study documents (IRB protocols, informed consent forms), updating and maintaining clinicaltrials.gov, preparing materials required for DSMB meetings, coordinating facility maintenance and regulatory compliance (clinical study room and office space), and maintaining radioactive study binders. The manager will coordinate various research studies and oversee activities such as ordering supplies, including radioactive tracers, maintaining stock/inventory, creating and disseminating study schedules, and updating Oncore to ensure research subject enrollment payment.