The Per Diem Clinical Research Coordinator performs the regular duties of a full- or part-time Clinical Research Coordinator on an as-needed basis. Because the role has a limited number of hours, it does not apply for Exempt status as is normal in this group. The coordinator assists with clinical research studies by obtaining informed consent, collecting, maintaining, and organizing study information, and may perform phlebotomy. The role also assists with preparing grant applications and documents for submission and filing, including materials for the Institutional Review Board and Grants and Contracts Office.