Medpace, Inc. is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Stirling. The role supports daily regulatory submissions activities, timelines, and documentation throughout the trial management process.
You will collect, review, assemble submissions, liaise with research sites, and ensure compliance with regulations. A life sciences degree and at least two years' experience are required, with strong Microsoft Office skills and
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Regulatory Submissions Specialist — Clinical Trials in Stirling 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.
