Lead, Translational Scientific Writing

Bristol Myers Squibb; Alabama; Hybrid; USD 170,000 - 207,000; Full time

Benefits offered by this job

Wellbeing support

Retirement plan and insurance

Flexible Time Off

Job summary

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.

Qualifications

• Masters or PhD in Hematology/Oncology/Neuroscience or related field with 6-8 years in industry or an academic setting.
• Proven written and oral communication skills.
• Ability to interpret data and craft key communication points from tables, listings, graphs.
• Ability to clearly organize presentations of data into a clear narrative.
• Experience with regulatory submissions (e.g., IND, NDA/sNDA) required.

Responsibilities

• Ensure timely delivery for the TD writing book of work such as pre-clinical reports and Translational biomarker reports across disease areas.
• Establish annual publication goals and timelines with priority rankings for regulatory submissions.
• Support regulatory submissions and regulatory interactions, writing translational sections for regulatory responses.
• Collaborate with TD scientists and other functions to execute publications/reports/regulatory documents.
• Provide guidance to multi-disciplinary teams and senior management on scientific direction.

Skills

Written communication

Regulatory strategy

Cross-functional leadership

Scientific writing

Education

Master's or PhD in Hematology/Oncology/Neuroscience

Tools

CARA/VERITY documentation systems

Job description

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.