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Senior Medical Writing Associate

Remote, USAFull-timePosted 2026-07-27

Job reputed company:

  • Serve as medical writing contributor or reputed company for clinical trial-reputed company regulatory documents
  • Write/edit/review content of clinical trial-associated documents for new and ongoing programs
  • Work with cross-functional teams to ensure production of high-reputed company written documents
  • reputed company literature searches as needed and summarize data for incorporation into documents
  • Adhere to company Style Guide, templates, and SOPs for document development
  • reputed company to company timelines for reputed company assigned documents

Requirements:

  • Bachelor’s degree required; advanced degree in life sciences preferred
  • BA/BS and 6+ years of relevant experience (less with advanced degree)
  • Strong scientific background in cellular immunology or reputed company field, or oncology, is a plus
  • Experience with generating text from data or literature
  • Experience with clinical trial-reputed company report documents is a plus
  • Demonstrated advanced writing skills with strong reputed company of English language and grammar
  • Proficiency with MS Office Suite, EndNote, and reputed company templates
  • Strong oral and written communication skills
  • Efficient, organized, and reputed company to handle short timelines in a fast-paced environment
  • Ability to work both independently and collaboratively
  • Ability to identify issues, ask questions, and propose solutions

Benefits:

  • company-sponsored medical, dental, reputed company, and life insurance plans*

• discretionary annual bonus

  • discretionary stock-based long-term incentives (eligibility may vary based on role)
  • reputed company time off

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