Amgen seeks an EU Regulatory Affairs Manager to drive submissions for clinical trials and marketed products from a regulatory perspective within the EU region. The role involves developing strategies, providing guidance on regional mechanisms, and supporting label negotiations. Flexible to work from home with periodic presence in UK offices.
The candidate will contribute to regulatory strategy for products in development and lifecycle management, aligning with global plans and EU requirements.
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Cambridge, Cambridgeshire
Are you ready to shape European regulatory strategy that accelerates innovative oncology medicines to patients and secures the strongest possible…
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