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8 часов назад

Associate Director, Clinical Supply Chain (Oncology)

185 000 - 200 000$
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Clinical Supply Chain (Oncology): Building and optimizing end-to-end clinical supply chains for Olema’s oncology programs with an accent on global inventory, shipping, vendor oversight, packaging, labeling, and IRT systems. Focus on forecasting clinical demand, managing late-stage global studies, mitigating supply risks, and ensuring uninterrupted drug distribution.

Location: San Francisco or Cambridge office, United States; approximately 15% domestic or international travel required.

Salary: $185,000–$200,000 annually, plus equity, bonus, and benefits.

Company

hirify.global is a clinical-stage biopharmaceutical company developing therapies for breast cancer and other oncology indications.

What you will do

  • Plan, implement, build, and optimize end-to-end clinical supply chains for clinical programs.
  • Develop and implement global clinical supply chain strategies.
  • Manage global inventories, shipping, customs, and third-party manufacturers and logistics providers.
  • Develop and manage Interactive Response Technologies (IRT) systems and clinical label generation.
  • Oversee packaging, labeling, and distribution activities across multiple vendors.
  • Partner with Clinical Operations and study execution teams to forecast demand, manage risks, and maintain uninterrupted clinical drug supply.

Requirements

  • Bachelor’s degree required; Master’s degree preferred.
  • 8+ years of biotechnology or pharmaceutical industry experience in clinical supply chain management.
  • Experience with late-phase clinical development, global inventory management, third-party logistics, and forecast demand management.
  • Experience managing global, large, late-stage studies with standard-of-care drugs.
  • Strong experience with global shipping, customs, clinical labels, and IRT specifications.
  • Thorough knowledge of Good Manufacturing Practices (GMP), plus hands-on QMS and purchasing systems troubleshooting experience.

Nice to have

  • Prior experience in oncology trials using small molecules.
  • Master’s degree.

Culture & Benefits

  • Competitive compensation and benefits package, including equity and bonus.
  • Open, flexible, and friendly work environment.
  • Equal opportunity workplace that values diverse expertise, backgrounds, and experiences.
  • Opportunities to develop a long-term career within a growing oncology company.

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