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You'll be the primary regulatory CMC voice on cross-functional matrix teams, covering everything from early clinical trial applications through to new marketing authorizations, post-approval changes, and full lifecycle management. That means you won't
Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity. Contribute to medical monitoring activities and support ongoing assessment of
You will lead and define our medical strategy, ensuring that scientific integrity, regulatory compliance, and patient-centricity sit at the core of everything we do. Reporting directly to the Medical Director, you will provide senior medical leadership