Director, Global Scientific and Regulatory Documentation, Content Strategy
Bristol Myers Squibb · Warsaw, Poland
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Role summary
This director-level role oversees scientific writing teams and regulatory documentation strategies supporting the drug development pipeline. Responsibilities include managing writer resources and development, ensuring compliance with regulatory standards, driving process improvements, and championing generative AI applications in documentation workflows. The position requires collaboration across therapeutic areas and influence on regulatory practices throughout the organization.
Privacy & handoff
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