Lead, Translational Scientific Writing
Listed on 2026-09-30
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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.
As a Lead, Translational Scientific Writing, you will play an important part at Bristol Myers Squibb in AL, United States.
Step into the Lead, Translational Scientific Writing role at Bristol Myers Squibb in AL, United States and grow with us.
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If your experience matches this role, we encourage you to apply.
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