Назад
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4 дня назад

Associate Director, Clinical Supply Chain

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 (Clinical Trials/AI): Leading end-to-end clinical supply chain strategy for global programs, from early-phase processes through complex Phase III pivotal trials, with an accent on forecasting, packaging, distribution, inventory, and IRT/RTSM systems. Focus on scaling manufacturing and logistics, managing global vendors and depots, building AI-enabled workflows, and ensuring uninterrupted patient supply across registrational trials.

Location: Remote within the United States, with Salt Lake City, Utah as the preferred home base. Remote employees must commit to regular on-site visits for routine work and departmental events.

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 benefits.

Company

hirify.global is a clinical-stage TechBio company developing investigational medicines through an AI-native platform that integrates biology, chemistry, and clinical development.

What you will do

  • Lead end-to-end clinical supply chain strategy for global programs from Phase I/II through Phase III pivotal trials.
  • Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management.
  • Manage external packaging vendors, contract manufacturing organizations, and global trial supply depots.
  • Design, implement, and optimize IRT/RTSM logic for flexible and complex trial designs.
  • Build data-driven and AI-enabled workflows, scalable supply chain tools, SOPs, and risk-mitigation strategies.
  • 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 management experience in the pharmaceutical or biotech industry.
  • Direct experience managing clinical supply chains for late-stage Phase IIb/III pivotal trials.
  • 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.
  • Experience managing contract packaging vendors, global depots, and clinical supply budgets.
  • Strong communication skills and the ability to work across cross-functional teams while navigating early-phase ambiguity and late-stage operational rigor.

Culture & Benefits

  • Values bold, ethical decision-making, direct engagement, active learning, urgency, ownership, and cross-functional collaboration.
  • Provides annual bonus eligibility, equity compensation, and a comprehensive benefits package.
  • Supports a remote work arrangement within the United States with regular on-site visits.
  • Uses AI in the hiring process to assist with application review; final decisions are made by human recruiters and hiring managers.

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