8 дней назад
Clinical Supply Chain Manager (AI)
62 400 - 84 000GBP
Мэтч & Сопровод
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Описание вакансии
Текст:
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
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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