Location: Maidenhead
Work Mode: Hybrid
Requisition ID: 3090
Description
Alnylam is looking for a Senior Manager of Medical Writing to join our team in Maidenhead. This role is responsible for the preparation of complex clinical and regulatory documents to support the development and registration of our innovative therapies. You will work closely with cross‑functional teams to ensure that all documentation meets high standards of quality, clarity, and compliance with international regulatory requirements.
Key Responsibilities
* Lead the authoring and editing of clinical study reports, protocols, investigator brochures, and summary documents for regulatory submissions.
* Manage the medical writing process for specific projects, ensuring timelines and quality standards are met.
* Collaborate with clinical, regulatory, and biostatistics teams to interpret and present complex data accurately.
* Ensure all documents adhere to ICH guidelines, company SOPs, and style guides.
* Provide strategic input into document development and submission planning.
* Manage external vendors and freelance writers as required.
Benefits
* Our benefit offerings are carefully chosen to help support your physical and mental health.
* Save money, protect your income and invest for the future through our financial resources and tools.
* We offer a variety of resources to support you in your every day life.
The benefits we offer may vary based on where you are on the globe but our commitment to your well-being, health and safety never changes.
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