Alnylam Pharmaceuticals in Maidenhead seeks an Associate Director of Regulatory Affairs to lead regulatory strategy for mid/late-stage CNS programs. The role involves coordinating regulatory submissions, serving as EU Regional Lead, and engaging with cross-functional teams. Candidates should have a Bachelor's degree with at least 6 years of experience in regulatory affairs within the biotechnology or pharmaceutical industry. Strong project management, communication, and strategic thinking skills are essential. Alnylam values alignment with its core values and offers a collaborative environment.
#J-18808-Ljbffr