Lead, Translational Scientific Writing
Listed on 2026-09-28
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Research/Development
Research Scientist, Regulatory Compliance Specialist
Bristol Myers Squibb in New Jersey is seeking an Associate Director of Scientific Writing to lead translational and regulatory documentation across late-stage development. You will oversee biomarker reports, translational sections for regulatory submissions, and coordination with global disease teams.
The role requires a PhD or MD with 6–8 years in industry, strong writing and communication skills, and ability to manage cross-functional projects in a fast-paced environment.
Consider building your career as a Lead, Translational Scientific Writing at Bristol Myers Squibb.
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This posting is for the Lead, Translational Scientific Writing role at Bristol Myers Squibb, based in AL, United States.
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