Alnylam Pharmaceuticals in the United Kingdom is seeking a Senior Manager of Regulatory Affairs to lead EU and international regulatory submissions, coordinating with EU/global leads and cross-functional teams. You will influence regulatory strategy and ensure timely submissions across product life cycles.
You will author/write portions of submissions when needed and manage filing processes, staying updated on EU requirements while liaising with internal teams and CROs.
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Senior Regulatory Affairs Manager — EU & Global Submissions 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.
