Strategic EU/Global Regulatory Submissions Lead
Listed on 2026-10-17
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Pharmaceutical
Alnylam Pharmaceuticals seeks a Senior Manager of Regulatory Affairs to drive EU and global submissions, aligning with cross-functional teams from development to registration. You will contribute to regulatory strategy and represent regulatory in product subteams, coordinating paper and electronic submissions and monitoring EU requirements.
The role requires coordinating responses to HA inquiries, maintaining regulatory files, and providing regulatory intelligence across programs.
This is a genuine role to take on the Strategic EU/Global Regulatory Submissions Lead role at Alnylampharmaceuticals.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 70..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Strategic EU/Global Regulatory Submissions Lead role in the description above.
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