Director Biostatistics

Bristol Myers Squibb

Princeton, NJ, US
Base: $218,740 - $296,867; bonus/equity: incentive...
50% onsite
Phd in statistics or biostatistics
9+ years clinical trials experience
Sas r or python programming proficiency
Bristol Myers Squibb is seeking a Director of Biostatistics to lead and innovate clinical trial designs that support regulatory approval and market access. The ideal candidate will possess significant experience in statistics or biostatistics, along with strong leadership and communication skills

Job Summary

  • The Director of Biostatistics drives the design of innovative clinical trials to support regulatory approval and market access within a diverse therapeutic pipeline.
  • This role requires leading cross-functional teams to present complex statistical solutions to governance bodies and external regulatory agencies.
  • Bristol Myers Squibb offers competitive compensation ranging from $218,740 to $296,867 depending on location, along with comprehensive health and wellbeing benefits.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Director of Biostatistics to lead and innovate clinical trial designs that support regulatory approval and market access. The ideal candidate will possess significant experience in statistics or biostatistics, along with strong leadership and communication skills.

Salary

Base: $218,740 - $296,867; Bonus/Equity: Incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • PhD in Statistics or Biostatistics
  • 9+ years clinical trials experience
  • SAS R or Python programming proficiency
  • Regulatory agency interaction experience
  • Direct management of statisticians

Nice-to-have

  • Experience with oncology or hematology
  • Strong communication and presentation skills
  • Culture of inclusiveness and diversity
  • Strategic workforce planning abilities
  • Global regulatory submission expertise

Key Requirements

  • PhD (9+ years) or MS (11+ years) in Statistics
  • At least 3 years of direct or matrix management experience
  • Proficiency in SAS, R, or Python for advanced statistical analysis
  • Proven track record in global regulatory agency interactions
  • Experience in drug development and pharmaceutical industry standards

Work Rights

Not specified

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