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.
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