Principal Scientist, Translational Research - Translational Safety Strategy

Bristol Myers Squibb

Seattle, WA, United States
Base: $152,360 - $184,628; bonus/equity: + incenti...
50% onsite
Car t cell therapy expertise
Immunology, molecular/cell biology, virology
Translational safety strategies
Lead end-to-end translational safety strategies, testing, and reporting across multiple assets and platforms, spanning clinical and commercial programs, ensuring critical alignment with research, clinical development, and medical affair objectives

Job Summary

  • Lead end-to-end translational safety strategies, testing, and reporting across multiple assets and platforms, spanning clinical and commercial programs, ensuring critical alignment with research, clinical development, and medical affair objectives.
  • Oversee complex testing operations, including sample testing workflows, case tracking, data flow, and data management operations; lead in-depth complex case investigations across clinical and commercial settings with scientific rigor and operational precision.
  • Provide scientific leadership and interpretation, integrating translational safety data to inform critical clinical and regulatory decision-making; serve as a subject matter expert contributing scientific insights to health authority inquiries and regulatory submissions.

Matching Summary

Lead end-to-end translational safety strategies, testing, and reporting across multiple assets and platforms, spanning clinical and commercial programs, ensuring critical alignment with research, clinical development, and medical affair objectives.

Salary

Base: $152,360 - $184,628; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • CAR T cell therapy expertise
  • Immunology, molecular/cell biology, virology
  • Translational safety strategies
  • Gene-modified CAR T cell product safety
  • Regulatory guidelines adherence
  • Clinical and commercial programs oversight

Nice-to-have

  • Collaborative and detail-oriented
  • Scientific rigor and operational precision
  • Continuous process improvements
  • Cross-functional efficiency
  • Subject matter expert
  • Fast-paced, highly matrixed environment

Key Requirements

  • Bachelor’s Degree 8+ years experience
  • Master’s Degree 6+ years experience
  • Ph.D. or equivalent 4+ years experience
  • Ph.D. 7+ years combined experience clinical trial research and basic sciences
  • Strong working knowledge of regulatory frameworks

Work Rights

Not specified

Tailored Resume

Cover Letter