Alnylam Pharmaceuticals is seeking an Associate Director of Regulatory Affairs Strategy to serve as EU Regional Lead for mid/late-stage CNS programs. You will coordinate EU regulatory submissions to EMA, work with the Global Regulatory Lead, and guide regulatory strategy across product development.
The role involves leading regulatory activity on subteams, providing regulatory intelligence, and liaising with CROs and internal departments.
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EU Regulatory Strategy Lead for CNS Programs 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.
