Global Regulatory Submissions Leader

Medpace, a full-service clinical contract research organization (CRO), provides phase I–IV development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Medpace employs thousands across 40+ countries and partners with clients to accelerate safe, effective therapeutics.

This role focuses on global start-up management, quality checks on submission documents, informed consent form approval, regulatory review, and presenting at bid defenses

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