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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Global Regulatory Submissions Lead for Clinical Trials in City of London employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those looking to kickstart their career in clinical trials, offering comprehensive onboarding and training that empowers you to become a data monitoring expert. With a strong emphasis on cross-functional collaboration and a supportive work culture, employees are encouraged to grow and develop their skills in a dynamic environment. Located in a vibrant office setting, Medpace provides a unique opportunity to contribute meaningfully to impactful projects while enjoying a fulfilling work-life balance.
