Senior Director, Biostatistics

Bristol Myers Squibb

Princeton, NJ, US
Base: $249,480 - $302,305; bonus/equity: + incenti...
Hybrid (50% onsite)
Lead biostatistics and dqs functions
Develop statistical analysis plans
Manage global cross-functional teams
Bristol Myers Squibb is seeking a Senior Director of Biostatistics to lead statistical input and analysis in clinical development. The role emphasizes collaboration across global teams and offers a competitive compensation package along with a flexible work environment

Job Summary

  • The Senior Director serves as the quantitative authority on the global program team, translating complex data into clear, decision-shaping insights.
  • This role involves leading highly complex projects, developing strategies for the area managed, and providing in-depth analyses to senior management.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible work-life benefits.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Director of Biostatistics to lead statistical input and analysis in clinical development. The role emphasizes collaboration across global teams and offers a competitive compensation package along with a flexible work environment.

Salary

Base: $249,480 - $302,305; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health coverage, 401(k), paid time off, and wellbeing programs

Skills & Requirements

Must-have

  • Lead biostatistics and DQS functions
  • Develop statistical analysis plans
  • Manage global cross-functional teams
  • Ensure regulatory compliance in submissions
  • Provide expert statistical guidance

Nice-to-have

  • Inclusive culture where talent thrives
  • Proactive risk management skills
  • Adaptation of new statistical methodologies
  • High-achieving team collaboration
  • Strategic decision-making influence

Key Requirements

  • Experience leading statisticians and managers
  • Expertise in clinical development plans
  • Knowledge of regulatory requirements and guidance
  • Ability to manage resources and set priorities
  • Background in drug research and development

Work Rights

Not specified

Tailored Resume

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