Назад
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8 дней назад

Clinical Supply Chain Manager

125 800 - 169 100$
Формат работы
hybrid
Тип работы
fulltime
Грейд
middle
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
Clinical Supply Chain Manager (Clinical Trials/AI): Leading end-to-end clinical supply chain strategy and scaling demand forecasting, packaging, global distribution, logistics, and inventory management for increasingly complex pivotal trials with an accent on IRT/RTSM systems, vendor oversight, and data-driven workflows. Focus on building scalable SOPs and risk-mitigation tools, coordinating cross-functional clinical development activities, and maintaining uninterrupted patient supply through late-stage development.

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

Annual base salary: $125,800–$169,100 for Salt Lake City and other U.S. locations; $138,380–$186,010 for New York City, Boston, and the San Francisco Bay Area. Additional annual bonus and equity compensation are available.

Company

hirify.global is a clinical-stage TechBio company developing 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 development programs from Phase I/II through Phase III pivotal trials.
  • Manage clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory as trial footprints expand.
  • Oversee contract packaging vendors, CMOs, global trial supply depots, and clinical supply budgets.
  • Design and manage IRT/RTSM logic for flexible and complex trial protocols.
  • Build AI-enabled, data-driven workflows, scalable supply chain tools, SOPs, and proactive risk-mitigation strategies.
  • Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC teams to align supply planning with trial milestones and commercial readiness.

Requirements

  • Bachelor’s degree and at least five years of clinical project management or clinical supply chain experience in the pharmaceutical or biotech industry.
  • Direct experience managing clinical supply for late-stage Phase IIb/III pivotal trials, including manufacturing and packaging scale-up.
  • Strong 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 knowledge of cGMP, cGCP, and blinded operational protocols.
  • Experience managing contract packaging vendors, global depots, and clinical supply budgets.
  • Remote employees must be located in the United States and commit to regular on-site visits for routine work and departmental events.

Nice to have

  • Experience navigating early-phase research while applying late-stage operational rigor.
  • Growth mindset focused on innovation, continuous improvement, and risk mitigation.
  • Strong verbal and written communication skills for cross-functional alignment.

Culture & Benefits

  • Collaborative, cross-functional environment across clinical development, business development, science, and AI.
  • Annual bonus, equity compensation, and comprehensive benefits package.
  • Values emphasize integrity, ownership, rapid learning, experimentation, accountability, and patient impact.
  • Regular departmental events and on-site collaboration are part of the working model.

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