The Per Diem Clinical Research Coordinator performs the regular duties of a full- or part-time Clinical Research Coordinator on an as-needed basis. Due to the limited number of hours, this individual does not apply for Exempt status as is usual in this group. The role supports clinical research studies by obtaining informed consent; collecting, maintaining, 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.
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