Associate Director, Clinical Supply Chain

Olema Oncology

Boston, United States
Base: $185,000 - $200,000 annually; bonus/equity: ...
On-site
End to end clinical supply chain management
Global clinical supply chain strategies
Manage global inventories and shipping
As the Associate Director of Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs

Job Summary

  • As the Associate Director of Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.
  • Your work will primarily encompass end-to-end clinical supply chain management, including developing global strategies, managing global inventories, shipping, and third-party providers.
  • The role requires 10+ years of experience in clinical supply chain management, thorough knowledge of GMP, and excellent project management skills.

Matching Summary

As the Associate Director of Clinical Supply Chain, you will plan, create, implement, build, and optimize the clinical supply chain to ensure uninterrupted and timely clinical drug supply for Olema’s clinical programs.

Salary

Base: $185,000 - $200,000 annually; Bonus/Equity: equity, bonus; Benefits: benefits

Skills & Requirements

Must-have

  • End to end clinical supply chain management
  • Global clinical supply chain strategies
  • Manage global inventories and shipping
  • Develop and manage IRT systems
  • Oversight packaging and labeling
  • Identify supply chain risks

Nice-to-have

  • Fearlessly support, motivate, and challenge
  • Put people first work
  • Difference maker professionalism
  • Impeccable professional ethics
  • Entrepreneurial mindset

Key Requirements

  • Bachelor's degree required, Master's preferred
  • 10+ years of experience
  • Late phase clinical development experience
  • GMP knowledge
  • Global shipping and customs experience
  • Experience developing IRT specifications

Work Rights

Not specified

Tailored Resume

Cover Letter