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Recursion

Associate Director, Clinical Supply Chain

Recursion

. Lead end-to-end clinical supply chain strategy for assigned global programs .

Posted 9/19/2026full-timeLondon • United KingdomSenior💰 £84,000 - £98,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading clinical supply chain strategies, managing complex trial designs, and optimizing logistics and inventory management in the pharmaceutical and biotech sectors. Proficient in developing scalable tools and processes while ensuring compliance with regulatory standards.

Highest-signal resume keywords
Clinical Supply Chain ManagementIRT/RTSM System DesignCGMP/cGCP GuidelinesClinical Project ManagementGlobal Distribution Networks

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Demand ForecastingInventory ManagementLogistics OptimizationData-Driven WorkflowsRisk-Mitigation StrategiesPackaging Strategy DevelopmentTrial Supply ManagementBudget ManagementPhase IIb/III Trial ExperienceRegulatory Compliance
Soft Skills
Outstanding Communication SkillsGrowth MindsetInnovation FocusProblem-Solving Ability
Industry Keywords
Pharmaceutical IndustryBiotech IndustryClinical TrialsSupply Chain StrategyContract Packaging ManagementSOP DevelopmentGlobal Clinical Trial OperationsImport/Export Regulations

About the role

Key responsibilities & impact
  • Lead end-to-end clinical supply chain strategy for assigned global programs
  • Establish Phase I/II processes while building for Phase III pivotal-trial requirements
  • Oversee clinical demand forecasting, packaging, labeling, global distribution, logistics, and inventory management
  • Manage external packaging vendors, CMOs, and trial supply depots
  • Implement, scale, and optimize IRT/RTSM logic for flexible, complex trial designs
  • Build and improve data-driven workflows using AI and advanced tools
  • Optimize forecasting, inventory management, and logistics processes
  • Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
  • Align supply strategies with trial milestones and commercial readiness
  • Create scalable supply chain tools and SOPs
  • Develop proactive risk-mitigation strategies supporting registrational trials and uninterrupted patient supply
  • Report to the Director of Clinical Supplies as part of the Recursion Development Team

Requirements

What you’ll need
  • Bachelor's degree
  • Minimum of 5 years of clinical project management or clinical supply chain management experience in the pharmaceutical/biotech industry
  • Direct experience managing clinical supply chains for late-stage (Phase IIb/III) pivotal trials
  • Experience scaling manufacturing and packaging strategies for flexibility and speed
  • Deep knowledge of global clinical trial supply operations
  • Knowledge of country-specific import/export regulations and complex distribution networks
  • Hands-on experience designing and managing IRT/RTSM systems
  • Strong understanding of cGMP/cGCP guidelines and blinded operational protocols
  • Proven experience managing contract packaging vendors and global depots
  • Experience managing clinical supply budgets effectively
  • Ability to navigate early-phase research ambiguity while applying rigor to late-stage development
  • Growth mindset focused on innovation and continuous improvement
  • Outstanding verbal and written communication skills

Benefits

Comp & perks
  • Annual bonus
  • Equity compensation
  • Comprehensive benefits package
  • Remote work option
  • Regular on-site visits for routine work and departmental events
  • Equal opportunity employment
  • Accommodations available on request during the selection process