Lead Scientific Writing, Translational Development
Listed on 2026-10-01
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Research/Development
Regulatory Compliance Specialist -
Management
Regulatory Compliance Specialist
Bristol Myers Squibb seeks an Associate Director of Scientific Writing in Translational Development, NJ. You will lead writing for regulatory and translational documents, coordinating with TD scientists and global teams to support lifecycle management and publication goals.
The role emphasizes strong writing, data interpretation, and regulatory submission experience, with required advanced degree and 6–8 years in industry or academia.
Consider building your career as a Lead Scientific Writing, Translational Development at Bristol-Myers Squibb Co.
Our organisation is growing, and we are hiring a Lead Scientific Writing, Translational Development in Madison, NJ, United States.
This position is for the Lead Scientific Writing, Translational Development role at Bristol-Myers Squibb Co.
We are seeking a motivated Lead Scientific Writing, Translational Development to join Bristol-Myers Squibb Co in Madison, NJ, United States.
The Lead Scientific Writing, Translational Development position in the Bio & Pharmacology & Health, Other field is open for applications.
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