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The Senior Research Compliance Administrator, under general direction and in coordination with other offices, has the ability to provide efficient customer service through the drafting, reviewing, and negotiation of complex agreements, sponsored research contracts, non-disclosure agreements and associated amendments related to clinical research; has an understanding of human subjects requirements including AAHRPP standards related to contracts and informed consent documents. Experience with clinical trials administration, feasibility assessments and related proposals, grants, contracts, agreements, negotiations, budgets, or billing.