Назад
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8 дней назад

Associate Director, Clinical Supply Chain (Biotech)

84 000 - 98 900GBP
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 clinical 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 supply operations, managing global logistics and external vendors, building AI-enabled workflows, and ensuring uninterrupted patient supply across flexible trial designs.

Location: London, England, or remote within the United Kingdom; regular on-site visits are required

Annual base salary: £84,000–£98,900, 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.
  • Oversee clinical demand forecasting, packaging, labeling, distribution, logistics, and inventory management.
  • Manage external packaging vendors, contract manufacturing organizations, global depots, and clinical supply budgets.
  • Design, implement, and optimize IRT/RTSM logic for flexible and complex clinical trial designs.
  • Build data-driven and AI-enabled workflows for forecasting, inventory management, and logistics optimization.
  • Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC to support 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.
  • Deep knowledge of global clinical trial supply operations, 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.
  • Proven experience managing contract packaging vendors, global depots, and clinical supply budgets.
  • Strong communication, cross-functional collaboration, innovation, and continuous-improvement skills.

Culture & Benefits

  • Hybrid work with a remote opportunity within the United Kingdom and regular on-site visits for routine work and departmental events.
  • Annual bonus eligibility and equity compensation.
  • Comprehensive benefits package.
  • Values centered on integrity, ownership, rapid learning, urgency, accountability, and cross-functional collaboration.

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