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.
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Strategic EU/Global Regulatory Submissions Lead in Maidenhead employer: Alnylampharmaceuticals
Alnylam Pharmaceuticals is an exceptional employer, offering a dynamic work environment in the heart of the biotech industry. With a strong commitment to employee growth and a culture that values innovation and collaboration, team members are empowered to make meaningful contributions to cutting-edge CNS programs. The company's focus on regulatory excellence and adherence to core values ensures that employees are not only supported in their professional development but also engaged in impactful work that drives advancements in healthcare.
