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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London
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based, Regulatory Submissions Manager to…
London
In this role you will lead global start-up and regulatory submissions within Clinical Operations, ensuring quality and compliance across sites.
London
Present during bid defenses, general capabilities meetings, and audits. Extensive experience in clinical research, preferably with a CRO.
Stirling
Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based, Regulatory Submissions…
Stirling
Medpace, Inc. is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Stirling.
London
Medpace, a full-service clinical contract research organization (CRO), provides phase I–IV development services to the biotechnology…
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