Skills
Scientific writing
Regulatory documentation
Cross-functional collaboration
About the Role
Bristol Myers Squibb is seeking a Scientific Writer II at a manager level to help create clear, accurate, and compelling scientific content that supports our mission to improve patient lives. You’ll partner with cross-functional teams to translate complex scientific and clinical information into documents that meet regulatory and internal standards.
Responsibilities
- Author and/or manage development of scientific and regulatory writing deliverables
- Collaborate with scientific, clinical, and medical teams to gather, interpret, and structure technical information
- Ensure documents are accurate, compliant, and aligned to applicable guidelines and organizational style standards
- Oversee writing workflows, timelines, and quality checks for assigned projects
- Contribute to continuous improvement of writing processes and documentation practices
Requirements
- Demonstrated experience in scientific writing within regulated or healthcare environments
- Strong ability to interpret technical data and translate it into reader-friendly language
- Working knowledge of regulatory documentation expectations and quality standards
- Excellent written communication and attention to detail
- Experience leading or managing writing activities at a team or project level
Benefits
- Competitive benefits and programs designed to support your personal and professional goals
- Work-life balance and flexibility in a mission-driven environment
- Opportunities to grow alongside high-performing teams
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