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Supply Chain Manager
COMPASS Pathways. Lead end-to-end global supply chain operations across clinical trial and commercial business domains .
Posted 11/6/2026full-timeRemote • United States, United KingdomMid-LevelSenior💰 $130,000 - $170,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing global supply chain operations within clinical trial and commercial domains, ensuring compliance with regulatory requirements and effective project management. Strong ability to build relationships with stakeholders and vendors while overseeing critical path planning and risk management.
Highest-signal resume keywords
Global Supply Chain ManagementProject ManagementStakeholder ManagementGMP, GCP, GDP KnowledgeClinical Trial Procedures Understanding
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Supply Chain OperationsProject PlanningRisk ManagementManufacturing ManagementPackaging ManagementRegulatory ComplianceCritical Path PlanningBudget ManagementDrug Product ManagementIMPD Revisions
Soft Skills
Interpersonal SkillsMulti-tasking AbilityAdaptability to Changing Priorities
Industry Keywords
Clinical TrialCommercial Supply ChainStakeholder CollaborationDistribution PartnersSupply Chain Vendors
Tech Stack
Tools & technologiesGoogle Cloud PlatformReact
About the role
Key responsibilities & impact- Lead end-to-end global supply chain operations across clinical trial and commercial business domains
- Ensure processes and systems effectively manage manufacturing and supply chain of clinical trial and commercial materials
- Oversee on-time delivery of bulk drug product to distribution partners
- Ensure packaging, labelling, release and shipping meet project timelines
- Collaborate with clinical and commercial regulatory partners and distribution vendors to secure approvals and meet shipping deadlines
- Manage drug product shelf life and resupply to ensure continuity of clinical study site supply
- Contribute to revisions of IMPD
- Manage and establish collaborations with worldwide clinical and commercial supply chain vendors in line with regulatory requirements
- Build and maintain relationships with manufacturing and packaging partners
- Perform project management activities, including critical path planning, resources and budgets
- Identify risks, implement mitigation and controls, and monitor and report status
- Report to the Associate Director, Supply Chain and collaborate within the supply chain matrix team
Requirements
What you’ll need- Bachelor’s Degree or equivalent in a science, operations management, or closely related subject (or relevant industry experience)
- Commercial Supply Chain Project Management desirable
- Proven stakeholder management
- Working knowledge of GMP, GCP and GDP
- Project planning and risk management
- Ability to react to changing priorities
- Excellent interpersonal skills
- Ability to multi-task
- Understanding of clinical trial procedures
- Knowledge of commercial supply chain
- Employment rights in the country to which you are applying; employment visa sponsorship is not available
Benefits
Comp & perks- Base salary, discretionary bonus, and equity
- Flexibility and generous time off
- Parental and reproductive support
- Health and medical benefits
- Mental health and wellbeing benefits
- Financial health benefits
- Reasonable accommodation during the interview process