Medpace is seeking a Regulatory Submissions Coordinator to support our Regulatory Submissions team in a full-time, on-site role in the UK. The position requires coordinating start-up submissions, reviewing regulatory documents, and ensuring compliance with guidelines to accelerate clinical trial timelines.
The ideal candidate has a Life Sciences degree with at least 2 years of Regulatory Submissions experience and strong organizational and communication skills to manage timelines and collaborate
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Clinical Submissions Specialist (Regulatory & Start-Up) in Stirling employer: Medpace
Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.
