Director, Global Scientific and Regulatory Documentation, Content Strategy

R : Director, Global Scientific and Regulatory Documentation, Content Strategy

Bristol Myers Squibb is seeking an experienced leader to guide a team of scientific writers across therapeutic areas, ensuring the quality and compliance of regulatory documentation.

Responsibilities

• 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 regulatory, clinical, and safety documentation according to good documentation principles (organization, clarity, scientific standards), consistency between text and tabular presentations or graphical displays, and compliance with BMS documentation standards and worldwide r...