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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading clinical supply chain strategies for global programs, with a strong focus on managing late-stage clinical trials and optimizing IRT/RTSM systems. Proficient in developing scalable supply chain tools and risk-mitigation strategies while ensuring compliance with cGMP/cGCP guidelines.
Highest-signal resume keywords
Clinical Supply Chain ManagementIRT/RTSM System DesignLate-Stage Clinical Trial ExperienceCGMP/cGCP ComplianceVendor Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Project ManagementSupply Chain StrategyDemand ForecastingInventory ManagementData-Driven WorkflowsRisk Mitigation StrategiesBudget ManagementManufacturing and Packaging StrategiesGlobal DistributionRegulatory Knowledge
Soft Skills
Outstanding Communication SkillsGrowth MindsetInnovation Orientation
Tools & Technologies
AI ToolsSupply Chain ToolsSOP Development
Industry Keywords
Pharmaceutical IndustryBiotech IndustryClinical TrialsImport/Export RegulationsComplex Distribution Networks
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 complex trial designs
- Build and improve data-driven workflows using AI and advanced tools
- Partner with Clinical Operations, Quality Assurance, Regulatory, and CMC
- Create scalable supply chain tools and SOPs
- Develop proactive risk-mitigation strategies for registrational trials and uninterrupted patient supply
- Report to the Director of Clinical Supplies as part of Recursion's Development Team
Requirements
What you’ll need- Bachelor's degree with a minimum of 5 years of clinical project management or clinical supply chain management experience in the pharmaceutical/biotech industry
- Direct experience managing the clinical supply chain for late-stage (Phase IIb/III) pivotal trials
- Experience scaling up manufacturing and packaging strategies to enable 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 track record managing contract packaging vendors and global depots
- Experience managing clinical supply budgets effectively
- Ability to navigate early-phase research ambiguity while imposing rigor for late-stage development
- Growth mindset oriented toward innovation and continuous improvement
- Outstanding verbal and written communication skills
- Willingness/ability to make London a home base or work remotely from the United Kingdom or United States with regular on-site visits
Benefits
Comp & perks- Annual bonus
- Equity compensation
- Comprehensive benefits package
- Remote work option
- Regular on-site visits for routine work and departmental events
- Accommodations available on request for candidates taking part in all aspects of the selection process