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Clinical Research Coordinator
Summary: The Clinical Research Coordinator will be the main operational interface with study subjects during the conduct of a study. The CRC will participate in and manage all administrative aspects of clinical trials under the direction and supervision of the Manager, Clinical Study Management. The ideal candidate will have experience as a CRC at a clinical research site working in the fields of diabetes, metabolism, or endocrinology. Performs duties in accordance with ProSciento’s values, policies, and procedures. Essential Duties and Responsibilities will include the following. Other duties may be assigned at the company’s sole discretion. Communicates with study subjects regarding their study status and enrolment
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