Global Regulatory Submissions Lead Clinical Trials
Listed on 2026-10-28
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Research/Development
Regulatory Compliance Specialist, Clinical Research
Medpace, Inc. in the United Kingdom is seeking a Regulatory Submissions Manager to join our Clinical Operations team on a full-time, office-based basis.
You will oversee global start-up activities and manage submission documents to support trial execution. Ideal candidates have extensive clinical research experience (preferably with a CRO), knowledge of Clinical Trial Applications in Europe, and strong oral and written communication, plus a collaborative, leadership‑driven approach.
We are currently recruiting a Global Regulatory Submissions Lead for Clinical Trials for our team in City Of London, England, United Kingdom.
The position is based in City Of London, England, United Kingdom.
This opportunity is part of our work in Management & Operations.
The advertised compensation is 60.000 - 90.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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