Associate Director Scientific Writing
Bristol Myers Squibb · Giralda, NJ +1 more
Medical AffairsFull-time$171k–$207kCompany career page
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Role summary
Bristol Myers Squibb seeks an Associate Director of Scientific Writing for its Translational Development group in New Jersey. The role involves authoring regulatory documents, biomarker reports, and scientific communications for late-stage clinical programs across hematology, oncology, immunology, cardiovascular, and neuroscience therapeutic areas.
What they're looking for
- Master's or PhD in hematology, oncology, neuroscience, or related field
- 6-8 years industry or academic scientific writing experience
- Experience with regulatory submissions including IND, NDA, and sNDA
- Strong understanding of clinical, translational, and mechanistic data interpretation
- Familiarity with documentation systems such as CARA or VERITY
- Proven ability to manage scientific collaborations and cross-functional projects
- Excellent written and oral communication skills with attention to detail
What you'll be doing
- Author regulatory documents, biomarker reports, and translational sections for submissions and clinical summaries
- Establish annual publication goals, timelines, and priority rankings with translational development scientists
- Collaborate with clinical, non-clinical, and pharmacology teams to develop regulatory responses and scientific communications
- Review and organize scientific data into clear narrative formats with appropriate tables and visualizations
- Support recruitment and hiring of additional scientific writers as needed
Privacy & handoff
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