Senior Director, Solid Tumor Asset Lead, Translational Development

Bristol Myers Squibb

Cambridge, Massachusetts, US
Base: $243,500 - $330,476 depending on location; b...
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12+ years industry experience in translational capacity
Ph.d. in oncology or related field
Expertise in solid tumor oncology disease biology
** Bristol Myers Squibb is seeking a Senior Director, Solid Tumor Asset Lead in Translational Development, responsible for developing and executing innovative biomarker strategies in oncology. The ideal candidate will have extensive experience in translational research and a strong background in oncology, with excellent communication skills and the ability to work in a collaborative, matrixed environment. **

Job Summary

  • The role involves leading the development and execution of innovative biomarker strategies for late-stage clinical oncology programs in solid tumors.
  • Candidates will collaborate with diverse functional groups including clinical, medical, commercial, and regulatory teams to align translational plans with project goals.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible work-life balance options.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Director, Solid Tumor Asset Lead in Translational Development, responsible for developing and executing innovative biomarker strategies in oncology. The ideal candidate will have extensive experience in translational research and a strong background in oncology, with excellent communication skills and the ability to work in a collaborative, matrixed environment. **

Salary

Base: $243,500 - $330,476 depending on location; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive health, wellness, and paid time off packages included

Skills & Requirements

Must-have

  • 12+ years industry experience in translational capacity
  • Ph.D. in Oncology or related field
  • Expertise in solid tumor oncology disease biology
  • Experience with genomics and immune profiling platforms
  • Proven track record of regulatory submission authoring

Nice-to-have

  • Strong understanding of modality agnostic therapies
  • Experience managing external academic collaborations
  • Ability to influence global cross-functional teams
  • Knowledge of competitive therapeutic landscape scenarios

Key Requirements

  • Ph.D. in Oncology/Hematology
  • 12+ years of industry experience
  • In-depth knowledge of drug development process
  • Experience with IND/NDA regulatory documents

Work Rights

Not specified

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