Alnylam Pharmaceuticals, Inc. is seeking an Associate Director of Regulatory Affairs Strategy to act as the EU Regional Lead for mid/late-stage CNS programs and possibly Regulatory Program Lead for early programs.
You will guide EU regulatory strategy, coordinate EMA submissions, and collaborate with Global Regulatory Team across product development and trials. The role requires strong regulatory intelligence, submission oversight, and strategic planning to align with Alnylam Core Values.
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EU Regulatory Strategy Lead – CNS Programs in Maidenhead employer: Alnylam Pharmaceuticals, Inc.
At Alnylam, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of biostatistics. Our Maidenhead office provides a hybrid working model, allowing for flexibility while ensuring strong team engagement. We are committed to employee growth, providing opportunities for professional development and involvement in cutting-edge clinical trials that make a meaningful impact on healthcare.
Contact Details:
Alnylam Pharmaceuticals, Inc. Recruitment Team
