Associate Director, Clinical Supply Lead (csl)

Bristol Myers Squibb UK

Madison, NJ, US
Base: $159,210 - $192,929; bonus/equity: + incenti...
50% onsite
10+ years clinical supply chain experience
Bachelor's degree in pharmacy or supply chain
Expertise in cgxps and ich requirements
The Associate Director provides day-to-day direction for forecasting, planning, and end-to-end clinical supply chain activities across assigned compounds and studies

Job Summary

  • The Associate Director provides day-to-day direction for forecasting, planning, and end-to-end clinical supply chain activities across assigned compounds and studies.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial protection, and flexible work-life balance programs.
  • This role serves as the single point of accountability for clinical supply planning while collaborating closely with cross-functional teams to ensure seamless supply solutions.

Matching Summary

The Associate Director provides day-to-day direction for forecasting, planning, and end-to-end clinical supply chain activities across assigned compounds and studies.

Salary

Base: $159,210 - $192,929; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • 10+ years clinical supply chain experience
  • Bachelor's degree in Pharmacy or Supply Chain
  • Expertise in cGxPs and ICH requirements
  • Strategic clinical asset planning and forecasting
  • Cross-functional team leadership and collaboration

Nice-to-have

  • Experience with AI integration in supply ecosystems
  • Proven ability to drive operational excellence
  • Strong analytical and problem-solving skills
  • Background in complex global drug development

Key Requirements

  • 10+ years clinical supply chain or operational planning experience
  • Bachelor's degree in Pharmacy, Supply Chain Management, Business, or Pharmaceutical Sciences
  • Extensive knowledge of all phases of drug development
  • Strong background in cGxPs and ICH regulatory requirements

Work Rights

Not specified

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