Senior Translational Scientific Writing Lead

Bristol Myers Squibb EU Policy

Madison (NJ)

On-site

USD 171,000 - 207,000

Full time

2 days ago

Be an early applicant

Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Benefits offered by this job

Flexible Time Off

11 paid holidays

Job summary

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

Qualifications

PhD/MD level with 6–8 years in industry or academia.
Experience writing regulatory submissions (IND, NDA/sNDA) required.
Excellent written and oral communication skills.

Responsibilities

Write translational and regulatory documents (non-clinical summaries, translational sections, briefing books, CSRs).
Contribute to abstracts, posters, manuscripts and other scientific communications.
Collaborate with TD scientists and other functions to produce publications and regulatory documents.
Provide guidance on data presentation and narrative flow to ensure clarity and impact.
Support regulatory submissions and responses for TD programs.