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Alnylam Pharmaceuticals

Develops RNAi-based therapies for genetic diseases

Senior Manager, Medical Writing

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeUnited States$146.1k - $197.7k

About the Job

Requirements

  • A bachelor's degree in Life Science with relevant writing expertise, or in English or Communications with relevant science expertise.
  • At least 6 years of experience as a medical writer in a sponsor and/or contract research organization setting.
  • In-depth knowledge of Good Clinical Practices, FDA regulations, International Council for Harmonisation guidelines, and the drug development process.
  • Ability to manage multiple projects in a fast-paced, deadline-driven environment and complete writing assignments in a timely manner with attention to detail.
  • Proficiency with Microsoft Windows, Word, Excel, and PowerPoint.
  • Ability to travel approximately 10%.
  • Alignment with Alnylam's stated core values.

Responsibilities

  • Produce high-quality writing deliverables on time.
  • Independently plan, write, edit, and format clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries, and related documents.
  • Facilitate and manage efficient review and finalization of documents produced internally and/or externally by consultants, contractors, and vendors.
  • Represent Medical Writing on multiple early-phase project teams or specific late-phase project teams, and collaborate with the Director of Medical Writing to plan and resource upcoming writing deliverables.
  • Collaborate with Biometrics, Clinical Operations, Clinical Development, Regulatory Affairs, Pre-Clinical Development, Program Management, Research, Quality, Corporate Communications, and external stakeholders.
  • Serve as a subject matter expert for clinical documents and their production.
  • Contribute to the development and maintenance of standard operating procedures and templates.
  • Oversee the work of contract writers on the clinical program.

Desired Qualifications

  • Experience with regulatory submissions, including CTA, IND, NDA, or BLA, and knowledge of electronic Common Technical Document formatting.
  • Experience overseeing the work of contract writers.
  • An advanced degree and/or professional certification or credentials.

About the Company

Alnylam Pharmaceuticals

Develops RNAi-based therapies for genetic diseases

Alnylam Pharmaceuticals develops RNA interference (RNAi) therapeutics to silence disease-causing genes, aiming to treat rare genetic disorders. Its products work by using RNA molecules that block gene expression, reducing the impact of specific genetic diseases. The company differentiates itself by concentrating on RNAi-based drugs for rare diseases and by building a pipeline through large clinical programs and strategic partnerships, such as commercialization deals in the Gulf States and collaborations with investors. Revenue comes from approved drug sales, licensing agreements, strategic collaborations, and related services like genetic testing and counseling. The company’s goal is to advance and commercialize RNAi therapies to improve outcomes for patients with genetic disorders, expanding its portfolio through partnerships and investments.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2002

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