Associate Director, Companion Diagnostics & Bioanalysis

Bristol Myers Squibb

Princeton, NJ, US
Base: $162,860 - $197,348; bonus/equity: + incenti...
Hybrid (50% onsite)
Clia and gxp regulated laboratory experience
Companion diagnostic (cdx) program support
Ihc and molecular diagnostic assay platforms
Bristol Myers Squibb is seeking an Associate Director for Companion Diagnostics & Bioanalysis to lead the development and execution of clinical diagnostic assays in a regulated laboratory environment. The ideal candidate should have extensive experience in GxP environments and a strong background in oncology-focused precision medicine and companion diagnostics

Job Summary

  • The role provides scientific and operational leadership for the planning, development, validation, and execution of clinical diagnostic assays supporting precision medicine programs.
  • Candidates will partner cross-functionally with Clinical Operations, Regulatory Affairs, and Quality to deliver compliant diagnostic solutions aligned with clinical development timelines.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible work-life balance options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Companion Diagnostics & Bioanalysis to lead the development and execution of clinical diagnostic assays in a regulated laboratory environment. The ideal candidate should have extensive experience in GxP environments and a strong background in oncology-focused precision medicine and companion diagnostics.

Salary

Base: $162,860 - $197,348; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive health, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • CLIA and GxP regulated laboratory experience
  • Companion diagnostic (CDx) program support
  • 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
  • Mentoring and team development capabilities
  • Global regulatory inspection readiness experience

Key Requirements

  • Bachelor's degree required; MS/PhD preferred
  • 8+ years in GxP-regulated CDx/bioanalysis environments
  • Prior experience with CLIA-certified laboratories
  • Proven track record managing external vendors and budgets

Work Rights

Not specified

Tailored Resume

Cover Letter