Alnylam Pharmaceuticals seeks a Senior Manager of Regulatory Affairs to lead regulatory submissions and strategy across EU and international health authorities. You will collaborate with the Global/EU lead and cross-functional teams to plan, author where relevant, and deliver regulatory submissions throughout product life cycles.
The role involves coordinating responses to authority questions, maintaining regulatory files, and contributing to regulatory intelligence and SOP improvements.
#J-18808-LjbffrSenior Regulatory Affairs Manager - EU & Global Submissions in Maidenhead employer: Alnylam Pharmaceuticals
As an Associate Director in Brand Marketing for Rare Diseases, you will join a dynamic and innovative team dedicated to improving patients' lives through strategic marketing initiatives. Our company fosters a collaborative work culture that values employee growth, offering opportunities for professional development and the chance to make a meaningful impact in the rare disease space. Located in a vibrant international setting, we provide a supportive environment where your contributions are recognised and rewarded, making us an excellent employer for those seeking a fulfilling career in the pharmaceutical industry.
