Bristol Myers Squibb is seeking an Associate Director of Scientific Writing to lead translational and regulatory documentation in a US NJ/ Madison setting. You will craft biomarker reports, translational sections of clinical summaries, briefing books, CSRs and investigator brochures, while contributing to abstracts, posters, and manuscripts with TD scientists.
The role requires strong regulatory writing experience, ability to coordinate with global disease teams, and a track record of producing
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Senior Translational Scientific Writing Lead Job at Bristol Myers Squibb EU Poli
Bristol Myers Squibb EU Policy · Madison, NJ, USA ·
- Job type:
- Full Time