Medpace is seeking a Regulatory Submissions Coordinator to support day-to-day regulatory activities and ensure timely start-up submissions. You will maintain databases and collaborate with research sites to collect essential documents, supporting timelines from start-up through to study enrollment.
The role requires a Life Sciences degree, 2+ years of experience in regulatory submissions, and strong organization and communication skills.
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Normanton on Trent
We are currently seeking an experienced Regulatory Consultant to join a Clinical Trial Strategy & Submissions team in Maidenhead.
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