Ipsen Biopharm Ltd in the United Kingdom is seeking a Regulatory Submission Project Manager to plan, coordinate, and delivery high-quality regulatory submissions on a global scale. You will work closely with Regulatory Affairs, Clinical, Quality, and Manufacturing teams to align strategy and timelines.
The role requires strong project management skills, international submission experience, and a deep understanding of CTD/eCTD frameworks.
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Contact Details:
Ipsen Biopharmaceuticals Inc. Recruitment Team
