Director, Global Scientific & Regulatory Documentation Strategy

About the role

The Director of Global Scientific and Regulatory Documentation, Content Strategy will lead a team of scientific writers across multiple therapeutic areas. Reporting to senior R&D leadership, you will shape the creation, review and delivery of high‑quality regulatory, clinical and safety documentation that supports the company’s pipeline.

Key responsibilities

• Establish and grow a global team of scientific writers, assigning projects and creating development plans.
• Mentor writers on a variety of content types and ensure adherence to BMS documentation standards.
• Identify and implement process improvements to enhance content flow and quality.
• Collaborate with Therapeutic Area Leads to align documentation strategy with R&D priorities.
• Assess resource needs, allocate staff, and manage external documentation support when required.
• Review regulatory, clinical and safety documents for clarity, scientific accuracy and compliance with worldwide regulations.
• Recruit, train and evaluate scientific writers, setting performance standards and providing coaching.
• Support skill‑set development in response to pipeline, technological and regulatory changes.
• Lead or contribute to innovation projects applying new documentation technologies.

Required profile

• Proven leadership experience managing scientific writing teams in a pharmaceutical or biotech environment.
• Deep understanding of regulatory, clinical and safety documentation requirements.
• Strong ability to assess project resources and prioritize work according to R&D goals.
• Excellent communication and mentorship skills.

Required skills

What we offer

• Competitive benefits package and flexible work arrangements.
• Opportunities for career growth within a global, innovative organization.
• Access to cutting‑edge scientific programs and cross‑functional teams.