Director, Audit Strategy And Vendor Quality

Bristol Myers Squibb

Princeton, NJ, US
Base: $188,250 - $228,114; bonus/equity: + incenti...
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Global risk-based gcp audit strategy
Vendor quality oversight framework
Third-party risk management (tprm)
** Bristol Myers Squibb is seeking a Director of Audit Strategy and Vendor Quality in Princeton, NJ, responsible for developing and executing a global audit strategy focused on compliance with Good Clinical Practice (GCP). The ideal candidate will have extensive experience in quality assurance within clinical development and will lead vendor quality oversight and risk management efforts. **

Job Summary

  • The Director, GCP Audit Strategy and Vendor Quality is accountable for designing and executing a global, risk-based audit strategy to ensure compliance with Good Clinical Practice (GCP) requirements.
  • This role will drive robust vendor quality oversight across all clinical trial service providers in close partnership with Development Quality.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Director of Audit Strategy and Vendor Quality in Princeton, NJ, responsible for developing and executing a global audit strategy focused on compliance with Good Clinical Practice (GCP). The ideal candidate will have extensive experience in quality assurance within clinical development and will lead vendor quality oversight and risk management efforts. **

Salary

Base: $188,250 - $228,114; Bonus/Equity: Additional incentive cash and stock opportunities (based on eligibility) may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • global risk-based GCP audit strategy
  • vendor quality oversight framework
  • Third-Party Risk Management (TPRM)
  • ICH/GCP and global regulatory requirements
  • Quality by Design principles

Nice-to-have

  • innovative and transformative mindset
  • data science or advanced analytics experience
  • executive-level communication and influencing skills
  • automation and build efficiencies

Key Requirements

  • 12+ years in Quality Assurance or regulated clinical development
  • Proven leadership of global audit strategy
  • Experience leading complex investigations
  • Direct involvement in M&A, in-licensing, and due diligence
  • B.S. or M.S. in a scientific, health, IT, or quality-related discipline

Work Rights

Not specified

Tailored Resume

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