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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Global Regulatory Submissions Leader in London employer: Medpace
Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.
