Director, Global Scientific and Regulatory Documentation, Content Strategy

Responsibilities

• Support establishment and ongoing development of a team of scientific writers working across therapeutic areas.
• Guide writer assignments and development plans, and mentor scientific writers in a variety of content and document assignments.
• Take 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 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 selection and maintenance of external documentation support for documents not covered adequately by in‑house resources.
• Review regulatory, clinical, and safety documentation...