Join to apply for the Senior Manager, Medical Writing role at Alnylam Pharmaceuticals
1 week ago Be among the first 25 applicants
Join to apply for the Senior Manager, Medical Writing role at Alnylam Pharmaceuticals
Get AI-powered advice on this job and more exclusive features.
Location: Maidenhead, UK – Hybrid
Travel: Ability to travel approximately 10% is required
At Alnylam, we’re not just developing therapies - we’re redefining what’s possible in medicine. As pioneers of RNA interference (RNAi) therapeutics, we’ve opened the door to a revolutionary class of medicines that silence the genes behind serious diseases. Now, we’re looking for a
1808: Senior Manager, Medical Writing
Location: Maidenhead, UK – Hybrid
Travel: Ability to travel approximately 10% is required
At Alnylam, we’re not just developing therapies - we’re redefining what’s possible in medicine. As pioneers of RNA interference (RNAi) therapeutics, we’ve opened the door to a revolutionary class of medicines that silence the genes behind serious diseases. Now, we’re looking for a talented Medical Writer who shares our passion for innovation and excellence to play a pivotal role in shaping the documents that support our clinical development programs. This is a unique opportunity to contribute to life-changing science in a fast-paced, collaborative environment where innovation, excellence, and purpose converge.
If you’re driven by discovery, inspired by purpose, and ready to shape the future of medicine, this is your moment — and Alnylam is your place!
Reporting to the Director, Medical Writing for the UK, this hybrid role is based two days per week at our UK head office in Maidenhead, offering the flexibility of remote work alongside in-person collaboration.
Our global team consists of 19 dedicated professionals located across the UK, Cambridge (US), and Philadelphia (US). Together, we are united by a shared vision: Revolutionizing Medical Writing as we meet patients’ needs for new medicines. We deliver on this by embracing innovation, fostering cross-functional collaboration, and maintaining the highest standards of scientific and technical excellence. With a deep commitment to strategic leadership and transparency, we take pride in producing the documents that support and accelerate the journey of life-changing therapies to the people who need them most.
What You’ll Do…
In this role, you’ll take ownership of key clinical documents, ensuring they meet the highest scientific, regulatory, and quality standards. You’ll collaborate cross-functionally with experts from Clinical Development, Biometrics, Regulatory Affairs, and more - guiding the end-to-end process of document development, from planning through to finalization. You’ll also lead and mentor contract writers, help shape our internal processes, and act as a subject matter expert within the Medical Writing team.
Key Responsibilities
* Independently write and manage core clinical documents (protocols, IBs, CSRs, ISS/ISE, etc.)
* Deliver high-quality writing outputs on time and in compliance with all regulations and SOPs
* Lead document review and approval processes with both internal and external contributors
* Represent Medical Writing across multiple cross-functional project teams
* Collaborate with internal departments and external stakeholders to ensure scientific accuracy and clarity
* Provide guidance and oversight to contract writers
* Contribute to the development and maintenance of SOPs and document templates
About You…
You’re a subject matter expert; someone who can help translate complex science into compelling, clear, and compliant communications that support our regulatory and clinical goals. You're a proactive, detail-oriented communicator who thrives in a dynamic and mission-driven environment.
You will have…
Essential Qualifications, Skills & Experience
* 6+ years of experience as a medical writer in the sponsor and CRO setting
* Experience planning and writing clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents
* Experience of regulatory submissions (CTA/IND/NDA/BLA) - knowledge of eCTD formatting would be advantageous
* A bachelor's degree (or equivalent) in Life Science or comparable subject area, with relevant writing expertise or in English/Communications with relevant science expertise
* In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process
* Impeccable attention to detail and ability to complete writing assignments in a timely manner
* A strong track record of successfully managing multiple projects in a fast-paced and deadline-driven environment
Desirable Skills And Experience
* Advanced degree and/or professional certification/credentials
* Experience overseeing the work of contract writers would be beneficial
* Demonstrate clear alignment with Alnylam’s core values
Are you ready to be part of what’s next? Join us and help bring groundbreaking RNAi therapies to patients around the world.
Next Steps
This vacancy will be advertised from Friday, 9 th May with a scheduled closing date of Friday, 23 rd May – we welcome your application as soon as possible.
Additional Resources
The Medical Writing team sits within our Regulatory Affairs group – find out more, here:
Alnylam Regulatory Affairs: https://www.alnylam.com/regulatory-affairs
Working at Alnylam: https://www.alnylam.com/careers/working-at-alnylam
Who We Are: https://www.alnylam.com/careers/who-we-are
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Marketing, Public Relations, and Writing/Editing
Referrals increase your chances of interviewing at Alnylam Pharmaceuticals by 2x
Get notified about new Manager Medical Writing jobs in Maidenhead, England, United Kingdom.
Uxbridge, England, United Kingdom 2 weeks ago
Associate Director, X-TA Regulatory Medical Writing
High Wycombe, England, United Kingdom 4 days ago
Medical Lead (Ophthalmology) Clinical Development - Executive Director
Addlestone, England, United Kingdom 2 weeks ago
Medical Director, Clinical Development – Hematology/Oncology
Uxbridge, England, United Kingdom 1 week ago
Reading, England, United Kingdom 1 month ago
Manager, X-TA Regulatory Medical Writing
High Wycombe, England, United Kingdom 4 days ago
Senior Project Manager - CLS Scientific - German Speaker
Woking, England, United Kingdom 1 week ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr