Associate Director, Global Regulatory Docs & Content

Bristol-Myers Squibb Co; Princeton (NJ); On-site; USD 171,000 - 207,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible work arrangements

Job summary

Bristol-Myers Squibb Co is seeking an Associate Director, Global Scientific and Regulatory Documentation, Content Strategy in Princeton, NJ. You will author, coordinate, and drive strategic regulatory documents for immunology and cardiovascular assets, guiding teams through complex submissions.

The role emphasizes expert writing, global regulatory standards, and cross-functional collaboration to ensure timely, compliant submissions.

Qualifications

• PharmD/PhD/MD in a relevant scientific discipline or Master’s/Bachelor’s with approximately 10 years of pharmaceutical regulatory documentation.
• All PhD in biological sciences and PharmD candidates are considered.

Responsibilities

• Author complex regulatory documents (e.g., CTD summaries, Pediatric Investigational Plans) for global submissions.
• Lead or co-lead document strategy and content organization for complex submissions.
• Coordinate timelines and ensure high-quality, compliant documentation across development assets.

Skills

Regulatory writing

Document management

Timeline management

Cross-functional collaboration

Regulatory submissions

Education

PharmD/PhD/MD in relevant discipline

Master's/Bachelor's with regulatory docs experience

Tools

Document management system

Regulatory publishing tools

Job description

Bristol-Myers Squibb Co is seeking an Associate Director, Global Scientific and Regulatory Documentation, Content Strategy in Princeton, NJ. You will author, coordinate, and drive strategic regulatory documents for immunology and cardiovascular assets, guiding teams through complex submissions.

The role emphasizes expert writing, global regulatory standards, and cross-functional collaboration to ensure timely, compliant submissions.