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 and organizing study information, and potentially performing phlebotomy. The role also assists with preparing grant applications and related documents for Institutional Review Board and Grants and Contracts Office submissions.
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Career Level
Entry Level