Associate Director, Companion Diagnostics & Bioanalysis

Bristol Myers Squibb

Princeton, NJ, US
Base: $162,860 - $197,348; bonus/equity: + incenti...
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Clia and gxp regulated laboratory experience
Companion diagnostic (cdx) program leadership
Ihc and molecular diagnostic assay platforms
** Bristol Myers Squibb is seeking an Associate Director for Companion Diagnostics & Bioanalysis in Princeton, NJ. This role focuses on providing scientific and operational leadership in developing and executing clinical diagnostic assays to support precision medicine initiatives. **

Job Summary

  • This role provides scientific and operational leadership for the planning, development, validation, and execution of clinical and translational diagnostic assays supporting precision medicine programs.
  • The position requires managing external vendors and CROs while ensuring compliance with regulatory expectations and delivering high-quality diagnostic solutions aligned with clinical timelines.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible work-life balance options to support employee goals.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking an Associate Director for Companion Diagnostics & Bioanalysis in Princeton, NJ. This role focuses on providing scientific and operational leadership in developing and executing clinical diagnostic assays to support precision medicine initiatives. **

Salary

Base: $162,860 - $197,348; 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

  • CLIA and GxP regulated laboratory experience
  • Companion diagnostic (CDx) program leadership
  • IHC and molecular diagnostic assay platforms
  • qPCR, ddPCR, NGS, and flow cytometry expertise
  • Vendor and CRO management in pharma settings

Nice-to-have

  • Oncology-focused precision medicine background
  • Cross-functional stakeholder influence skills
  • Culture of integrity, inclusion, and innovation
  • Global diagnostic platform provider engagement

Key Requirements

  • Bachelor's degree required; MS/Ph.D. preferred
  • 8+ years in GxP-regulated CDx/bioanalysis environments
  • Prior experience with CLIA-certified laboratories
  • Proven track record in oncology precision medicine

Work Rights

Not specified

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