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Director / Senior Director, Medical Writing
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$217,279 - $274,868 a year
Full-time
- Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in partnership with a talented and collaborative team across our Research/Pre-Clinical, CMC, Regulatory, Clinical, and Quality organizations to author and drive development of key documents in support of all of our Phase 1 through Phase 3 programs.
- This role will be responsible for the build of critical writing infrastructure and processes at Annexon, including the development of best practices and resources for document management and timelines, template and shell creation, lexicon and document QC, publishing, and editing standards.
- You will also have an opportunity to support scientific communications, including the creation of manuscripts, abstracts and posters for congresses and external publication.
- Prior work history at a biotech or pharmaceutical company preferred, smaller company environment ideal
- and data visualization (e.g., Spotfire, etc.)
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