Senior Director, Solid Tumor Asset Lead, Translational Development

Bristol Myers Squibb

Cambridge, Massachusetts, US
Base: $243,500 - $330,476; bonus/equity: + incenti...
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12+ years industry experience in translational capacity
Ph.d. in oncology or related field
Solid tumor oncology disease biology knowledge
** Bristol Myers Squibb is seeking a Senior Director, Solid Tumor Asset Lead for Translational Development, responsible for developing and executing translational strategies in solid tumor oncology. The ideal candidate will possess a Ph.D. in Oncology or a related field, with over 12 years of industry experience and a strong background in translational research and biomarker strategies. **

Job Summary

  • The role is responsible for developing and executing translational strategies and innovative biomarker plans for late-stage solid tumor oncology programs.
  • Candidates must possess a Ph.D. in Oncology or related field with over 12 years of industry experience, including significant time in a translational capacity.
  • The position offers competitive compensation ranging from $243,500 to $330,476 depending on location, along with comprehensive health coverage and flexible work-life benefits.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Director, Solid Tumor Asset Lead for Translational Development, responsible for developing and executing translational strategies in solid tumor oncology. The ideal candidate will possess a Ph.D. in Oncology or a related field, with over 12 years of industry experience and a strong background in translational research and biomarker strategies. **

Salary

Base: $243,500 - $330,476; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • 12+ years industry experience in translational capacity
  • Ph.D. in Oncology or related field
  • Solid tumor oncology disease biology knowledge
  • Biomarker strategy development and execution
  • Clinical protocol authoring and regulatory submissions

Nice-to-have

  • Experience with modality agnostic therapies
  • Strong publication record as major contributor
  • Ability to influence global cross-functional teams
  • Knowledge of genomics and immune profiling platforms

Key Requirements

  • Ph.D. in Oncology/Hematology
  • 12+ years of industry experience
  • Proven track record in biomarker strategy implementation
  • Experience with regulatory document submission (INDs/NDAs)

Work Rights

Not specified

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