Medpace, a leading global clinical research organization, is seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team in the United Kingdom. You will oversee global start-up activities and ensure regulatory documents meet quality standards.
The role emphasizes collaboration across functions, timely submissions, and adherence to regulatory requirements in Europe. You will present at meetings and audits, drive process improvements, and mentor project
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Global Regulatory Submissions Lead 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.
