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Clinical Research Associate
Job SummaryUnder general direction, is responsible for analysis and understanding of the critical documents that are associated with clinical research, including: protocols, amendments, consent forms, contracts and budgets to ensure research billing compliance and sound financial management of clinical research; performs initial review of clinical trials submitted to Clinical Trials Office, performs research billing compliance reviews; is responsible for abstraction of medical and research record documentation to ensure timely and accurate coding of all medical and research study services, and has general knowledge of CMS and Third Party Payer billing rules; interfaces with various departments, physicians, clinical research nurses, coordinators, sponsors and local h


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