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3 дня назад

Associate Director, Clinical Supply Chain (Biotech)

186 010 - 218 790$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
UK/US/Canada
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 (Biotech): Leading end-to-end clinical supply chain strategy for global pharmaceutical and biotech programs with an accent on pivotal trials, forecasting, packaging, distribution, and inventory management. Focus on scaling Phase I/II processes for Phase III trials, optimizing IRT/RTSM systems, managing global vendors and logistics, and building AI-enabled supply workflows.

Location: Remote within the United States, with Salt Lake City as the ideal home base and regular on-site visits required

Annual base salary: $186,010–$218,790 in New York City, Boston, and the San Francisco Bay Area; $169,100–$198,900 in Salt Lake City and other U.S. locations. The role is also eligible for an annual bonus, equity compensation, and comprehensive benefits.

Company

hirify.global is a clinical-stage biotech company using AI, biology, chemistry, automation, data science, and engineering to develop medicines for oncology, rare disease, neuroscience, immunology, and other therapeutic areas.

What you will do

  • Lead end-to-end clinical supply chain strategy for global programs, establishing Phase I/II processes that can scale to Phase III pivotal trials.
  • Manage clinical demand forecasting, packaging, labeling, international distribution, logistics, and inventory as trial footprints expand.
  • Oversee contract packaging vendors, contract manufacturing organizations, global depots, clinical supply budgets, and trial supply operations.
  • Design and optimize IRT/RTSM logic to support flexible and complex trial designs.
  • Build data-driven workflows using AI and advanced tools to improve forecasting, inventory management, and logistics.
  • Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC to align supply strategies with trial milestones and commercial readiness.

Requirements

  • Bachelor’s degree and at least 5 years of clinical project management or clinical supply chain experience in the pharmaceutical or biotech industry.
  • Direct experience managing clinical supply chains for late-stage Phase IIb/III pivotal trials, including manufacturing and packaging scale-up.
  • Deep knowledge of global clinical trial supply operations, country-specific import/export regulations, and complex distribution networks.
  • Hands-on experience designing and managing IRT/RTSM systems, with strong knowledge of cGMP, cGCP, and blinded operational protocols.
  • Ability to manage contract packaging vendors, global depots, clinical supply budgets, and cross-functional alignment.
  • Remote employees must be based in the United States and commit to regular on-site visits.

Culture & Benefits

  • Work in an execution-focused development organization advancing investigational medicines toward commercialization.
  • Values include integrity, direct collaboration, active learning, urgency, ownership, accountability, and cross-functional teamwork.
  • Annual bonus, equity compensation, and a comprehensive benefits package.
  • AI is used in the hiring process to help review applications, while final decisions remain with human recruiters and hiring managers.

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