Full-time

Director, Global Scientific and Regulatory Documentation, Content Strategy

Posted by Bristol-Myers Squibb • June 10, 2026

📍 bogotá, bogotá, d.c., Colombia
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Description

Director, Global Scientific and Regulatory Documentation, Content Strategy (Requisition R ).

Responsibilities

  • Supports the establishment and ongoing development of a team of scientific writers working across therapeutic areas.
  • Guides writer assignments and development plans, and mentors scientific writers in a variety of content and document assignments.
  • Takes initiative to create and implement process improvements and behavioral changes that support the quality and content flow of information supporting the BMS pipeline.
  • Work with Therapeutic Area Lead to optimize the delivery of content and documentation that supports the BMS pipeline.
  • Assess resource requirements for all projects, assign resources according to BMS R&D priorities, and prepare criteria and strategies for the selection and maintenance of external documentation support for documents not covered adequately by in-house resources.
  • Review...

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