Senior Director, Solid Tumor Asset Lead, Translational Development

Bristol Myers Squibb

Cambridge, Massachusetts, US
Base: $243,500 - $330,476; bonus/equity: + incenti...
Hybrid (50% onsite)
12+ years industry experience in translational capacity
Ph.d. in oncology or related field
Solid tumor oncology disease biology knowledge
The Senior Director, Solid Tumor Asset Lead position at Bristol Myers Squibb involves leading translational strategies in solid tumor oncology, focusing on innovative biomarker strategies and cross-functional collaboration. The role requires extensive experience in oncology and translational research, with a strong emphasis on communication and project leadership

Job Summary

  • The role is responsible for developing and executing translational strategies in solid tumor oncology, including innovative biomarker strategies for patient selection and resistance.
  • Candidates must possess a Ph.D. in Oncology or related field with over 12 years of industry experience, specifically in translational capacities.
  • The position offers competitive compensation ranging from $243,500 to $330,476 depending on location, along with comprehensive health coverage and flexible time off benefits.

Matching Summary

Match Score: 88

The Senior Director, Solid Tumor Asset Lead position at Bristol Myers Squibb involves leading translational strategies in solid tumor oncology, focusing on innovative biomarker strategies and cross-functional collaboration. The role requires extensive experience in oncology and translational research, with a strong emphasis on communication and project leadership.

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 wellness programs

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 external academic collaborators
  • Experience working in matrixed industrial environment

Key Requirements

  • Ph.D. in Oncology/Hematology
  • 12+ years of industry experience
  • In-depth understanding of solid tumor oncology
  • Proven track record of writing scientific articles
  • Working knowledge of genomics and immune profiling platforms

Work Rights

Not specified

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