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Associate Director Medical Writing Job at Meet Life Sciences in San Francisco Ba

Meet Life Sciences, San Francisco Bay Area, United States


Associate Director, Medical Writing (Hybrid - SF Bay Area)


We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs. This individual will play a key role in shaping document strategy, ensuring scientific accuracy, and driving cross-functional alignment across clinical, regulatory, and biostatistics teams.


This is a hybrid role based in the San Francisco Bay Area. Relocation package is available.


Key Responsibilities

  • Lead the planning, authoring, and review of clinical and regulatory documents, including clinical study reports (CSRs), protocols, investigator brochures (IBs), and submission documents
  • Serve as the medical writing lead on complex, multi-phase programs, including late-stage development and regulatory submissions
  • Collaborate cross-functionally with Clinical Development, Regulatory Affairs, Biostatistics, and Clinical Operations to ensure aligned messaging and data interpretation
  • Drive document strategy and timelines to support IND, NDA, and other global regulatory submissions
  • Ensure all documents meet regulatory requirements, internal standards, and industry best practices
  • Manage external medical writers and vendors as needed
  • Provide mentorship and guidance to junior writers and cross-functional team members
  • Contribute to process improvements and development of templates, style guides, and best practices


Qualifications

  • PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required
  • 8+ years of medical writing experience within biotech, pharma, or CRO environments
  • Demonstrated experience supporting complex clinical development programs and regulatory submissions (IND, NDA, BLA, etc.)
  • Strong expertise in authoring clinical and regulatory documents (e.g., CSRs, protocols, IBs)
  • Proven ability to manage multiple writing projects and timelines in a fast-paced environment
  • Excellent written and verbal communication skills, with strong attention to detail
  • Experience working in cross-functional teams and influencing without direct authority
  • Prior leadership or mentoring experience preferred


If this role sounds of interest, please reach out to tanya.kochan@meetlifesciences.com.