Translational Writing Lead, Scientific Strategy

Bristol Myers Squibb; Madison (NJ); On-site; USD 110,000 - 160,000; Full time

Job summary

Bristol Myers Squibb, based in New Jersey, seeks a translational development writer to produce biomarker reports and regulatory documents and to support publications for regulatory submissions. The role collaborates with TD scientists globally to ensure timely delivery of manuscripts, abstracts, and briefing materials.

The incumbent will help craft translational sections for submissions, coordinate with cross-functional teams, and contribute to scientific communications across disease areas.

Qualifications

• Writes scientific documents including biomarker/regulatory reports.
• Supports abstracts, posters, manuscripts and other scientific communications arising from the group.
• Collaborates with global TD teams to coordinate publication plans and life-cycle activities.

Responsibilities

• Ensure timely delivery for the TD writing book of work such as pre-clinical reports and Translational biomarker reports across disease areas.
• With TD scientists, establish annual publication goals, publication plan with priority rankings, and timelines for submission.
• Supports regulatory submissions, regulatory interactions, writes translational sections for regulatory responses and queries for the TD group.
• Collaborate with TD scientists and representatives of other functions to execute publications/reports/regulatory documents.
• Collaborate with TD Scientists and review data to determine appropriate formats and improve flow and clarity of narrative.

Skills

Scientific writing

Regulatory documents

Biomarker reports

Clinical pharmacology

Publications

Tools

CARA

VERITY

Job description

Bristol Myers Squibb, based in New Jersey, seeks a translational development writer to produce biomarker reports and regulatory documents and to support publications for regulatory submissions. The role collaborates with TD scientists globally to ensure timely delivery of manuscripts, abstracts, and briefing materials.

The incumbent will help craft translational sections for submissions, coordinate with cross-functional teams, and contribute to scientific communications across disease areas.