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