Sr Manager, Medical Writing

Sr Manager, Medical Writing

Full-Time 60000 - 80000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Create high-quality medical documents and collaborate with diverse teams in the CNS field.
  • Company: Join a leading pharmaceutical company dedicated to innovation and inclusivity.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Other info: Dynamic role with global collaboration and a focus on quality and compliance.
  • Why this job: Make a real impact in healthcare while developing your writing and strategic skills.
  • Qualifications: Bachelor’s degree in Life Sciences or English/Communications; 6+ years of medical writing experience.

The predicted salary is between 60000 - 80000 £ per year.

The Senior Manager, Medical Writing will partner closely with cross-functional project teams to plan, develop, and deliver high-quality clinical and regulatory documents in compliance with global regulations, Good Clinical Practice (GCP), and internal SOPs. This role plays a key part within the Central Nervous System (CNS) therapeutic area, contributing both hands-on expertise and strategic oversight while collaborating with internal stakeholders and external partners. This hybrid position requires two days per week in our Maidenhead office.

Key Responsibilities

  • Produce high-quality, on-time medical writing deliverables across the clinical development lifecycle.
  • Independently plan, write, edit, and format key documents including clinical protocols, investigator brochures, clinical study reports, and integrated summaries of safety and efficacy.
  • Represent Medical Writing on CNS project teams, collaborating across functions to support program goals and timelines.
  • Facilitate efficient document review and finalisation processes for materials developed internally and/or by external vendors and contract writers.
  • Oversee and provide direction to contract medical writers, ensuring consistency, quality, and adherence to standards.
  • Engage confidently with a broad range of stakeholders, demonstrating strong stakeholder management, clear communication, and the ability to manage expectations with a sense of urgency.
  • Prepare effectively for cross-functional meetings and maintain a strong 'big-picture' mindset while delivering at pace.
  • Contribute to the development and maintenance of medical writing SOPs and templates.

Required Qualifications

  • Bachelor’s degree in Life Sciences with relevant writing expertise, or in English/Communications with strong scientific experience; advanced degree or professional certification preferred.
  • 6+ years of experience as a medical writer within a pharmaceutical organisation preferably.
  • In-depth knowledge of GCP, FDA regulations, ICH guidelines, and the drug development process.
  • Demonstrated ability to manage multiple priorities in a fast-paced, deadline-driven environment.
  • Proven ability to work collaboratively, communicate openly, and adapt writing style for different audiences.
  • Flexibility to work across global time zones, with the majority of stakeholders based in U.S. Eastern Time (EST).
  • High attention to detail and strong proficiency with Microsoft Word, Excel, and PowerPoint.

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity.

Sr Manager, Medical Writing employer: Alnylam Pharmaceuticals

At Alnylam, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of medical writing. Our Maidenhead office provides a supportive environment where employees can thrive, with opportunities for professional growth and development while contributing to groundbreaking projects in the Central Nervous System therapeutic area. We value diversity and inclusion, ensuring that every team member feels empowered and engaged in their work.
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Contact Detail:

Alnylam Pharmaceuticals Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Sr Manager, Medical Writing

✨Tip Number 1

Network like a pro! Reach out to your connections in the medical writing field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GCP, FDA regulations, and ICH guidelines. Be ready to discuss how your experience aligns with the responsibilities of the Senior Manager role, especially in the CNS therapeutic area.

✨Tip Number 3

Showcase your collaborative spirit! During interviews, highlight examples of how you've worked with cross-functional teams to deliver high-quality documents. This will demonstrate your ability to engage confidently with stakeholders.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in being part of our team at Alnylam.

We think you need these skills to ace Sr Manager, Medical Writing

Medical Writing
Clinical Protocols
Investigator Brochures
Clinical Study Reports
Integrated Summaries of Safety and Efficacy
Good Clinical Practice (GCP)
FDA Regulations
ICH Guidelines
Stakeholder Management
Clear Communication
Document Review and Finalisation
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Adaptability

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in medical writing, especially in the CNS therapeutic area. We want to see how your skills align with our needs, so don’t hold back on showcasing relevant projects!

Showcase Your Expertise: When detailing your qualifications, emphasise your knowledge of GCP, FDA regulations, and ICH guidelines. We’re looking for someone who can hit the ground running, so let us know how your background prepares you for this role.

Be Clear and Concise: In your written application, clarity is key! Use straightforward language and structure your documents well. We appreciate a good writer, so make sure your application reflects your ability to communicate effectively.

Apply Through Our Website: We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!

How to prepare for a job interview at Alnylam Pharmaceuticals

✨Know Your Documents Inside Out

Before the interview, make sure you’re familiar with the types of clinical and regulatory documents you'll be working on, like clinical protocols and study reports. Being able to discuss these confidently will show your expertise and readiness for the role.

✨Showcase Your Collaboration Skills

Since this role involves working closely with cross-functional teams, prepare examples of how you've successfully collaborated in the past. Highlight your ability to manage expectations and communicate clearly with various stakeholders.

✨Demonstrate Your Regulatory Knowledge

Brush up on GCP, FDA regulations, and ICH guidelines. Be ready to discuss how you’ve applied this knowledge in previous roles, as it’s crucial for producing high-quality medical writing deliverables.

✨Prepare for the Big Picture

During the interview, keep a 'big-picture' mindset. Be prepared to discuss how your work contributes to overall project goals and timelines, and how you can maintain quality while delivering at pace.

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