Associate Director, Regulatory Strategy

The Associate Director, Regulatory Strategy serves as the EU Regional Lead for mid/late-stage CNS programs and may lead early programs within the Alnylam pipeline. This role is responsible for planning and coordinating regulatory submissions to the EMA, representing Regulatory Affairs on cross-functional teams, and providing strategic regulatory advice for product development and registration. The position involves interpreting EU regulatory requirements, managing interactions with health authorities, and ensuring compliance with internal and external regulatory standards.