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Regulatory Submissions Specialist — Clinical Trials
Job in
Stirling, Stirlingshire, AB42, Scotland, UK
Listed on 2026-07-13
Listing for:
Medpace, Inc.
Full Time
position Listed on 2026-07-13
Job specializations:
-
Healthcare
Healthcare Compliance
Job Description & How to Apply Below
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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