The Clinical Research Coordinator I will participate in clinical research activities related to the All of Us study, a NIH initiative to enroll one million people across the U.S. to help build one of the most diverse health databases in history. The Clinical Research Coordinator I will be responsible for obtaining informed consent, collecting and processing biospecimens, performing some clinical assessments, and collecting, maintaining, and organizing study information. They will also assist in preparing documents (for e.g., Institutional Review Board, Grants and Contracts Office) and performing other study related activities as needed.