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8 дней назад

Clinical Supply Chain Manager (AI)

62 400 - 84 000GBP
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 (AI) (Clinical Trials/Global Logistics): Scaling end-to-end clinical supply operations from exploratory programs to complex global pivotal trials with an accent on demand forecasting, packaging, distribution, inventory management, and IRT/RTSM systems. Focus on designing scalable supply chain workflows, optimizing logistics with AI and advanced tools, and coordinating vendors and cross-functional teams to maintain uninterrupted patient supply.

Location: London, England, or remote within the United Kingdom with regular on-site visits for routine work and departmental events

Annual base salary: £62,400–£84,000, plus 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.
  • Manage clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory as trial footprints expand.
  • Oversee contract packaging vendors, CMOs, trial supply depots, and clinical supply budgets.
  • Design, implement, and optimize IRT/RTSM logic for flexible and complex trial designs.
  • Build scalable supply chain tools, SOPs, data-driven workflows, and risk-mitigation strategies using AI and advanced tools.
  • Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC to align supply strategies with trial milestones and commercialization.

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.
  • Outstanding written and verbal communication skills for cross-functional alignment.

Nice to have

  • Experience navigating early-phase research while applying the operational rigor required for late-stage development.
  • Growth mindset focused on innovation, agility, and continuous improvement.

Culture & Benefits

  • Values include integrity, direct collaboration, active learning, urgency, ownership, and accountability.
  • Remote employees can work from the United Kingdom with regular on-site participation.
  • Annual bonus, equity compensation, and a comprehensive benefits package are available.
  • Work takes place in a cross-functional development organization advancing medicines toward commercialization.

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