Medpace in London is seeking a Regulatory Submissions (Study Start-up) Manager to lead global start-up activities within our Clinical Operations team. The role focuses on coordinating regulatory submissions and ensuring timely approval across regions, while partnering with project teams.
The successful candidate will bring extensive clinical research experience, strong regulatory knowledge for Europe, and proven leadership to drive study start-up deliverables and audits.
#J-18808-Ljbffr
Global Regulatory Submissions Lead, Study Start-up 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.
