Executive Director, Clinical Supply Management

Jade Biosciences

. Provide strategic and operational leadership for Jade’s Clinical Supply Management function .

Posted 10/9/2026full-timeRemote • United StatesLead💰 $280,000 - $300,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in clinical supply chain management, particularly for biologics, with a strong focus on regulatory compliance, team leadership, and strategic planning. Proficient in managing complex supply processes, including cold-chain logistics and budget oversight, while ensuring adherence to global regulatory standards.

Highest-signal resume keywords

Clinical Supply Chain ManagementRegulatory ComplianceTeam LeadershipCold-Chain LogisticsBudget Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Supply ManagementBiologics ExperienceCGMPGDPGCPIRT/IxRS SystemsClinical Supply Forecasting ToolsRegulatory SubmissionsSOP DevelopmentSupply Chain Strategy

Soft Skills

LeadershipCommunicationInterpersonal SkillsProblem-SolvingMentoring

Industry Keywords

Life SciencesChemical EngineeringGlobal Regulatory RequirementsCold-Chain StorageClinical DevelopmentPhase 3 StudiesINDIMPDCTASupply Risk Management

Tech Stack

Tools & technologies

Google Cloud PlatformPug

About the role

Key responsibilities & impact

Provide strategic and operational leadership for Jade’s Clinical Supply Management function
Develop and scale the team through internal headcount and external partners, including recruiting, onboarding and mentoring team members and consultants
Develop business processes and SOPs with the Quality function
Define and implement clinical supply strategy for programs from Phase 1/2 through Phase 3, with forward planning for BLA filing, launch and commercial readiness
Build and maintain global demand forecasts and supply plans based on protocols, enrollment projections and site activation plans
Advise Senior Management and Clinical Operations and Development on supply risks and challenges
Collaborate with Clinical Operations, Clinical Development, Quality, Regulatory Affairs and CMC
Select, contract and manage clinical supply CMOs, depots, couriers, logistics providers and other critical suppliers
Oversee labeling, packaging, blinding, cold-chain storage and global distribution of drug products
Manage comparator sourcing, expiry extensions, relabeling, returns, reconciliation and destruction
Define IRT/IxRS supply requirements and resupply strategies; monitor depot and site inventory
Ensure compliance with SOPs, cGMP, GDP, GCP, ICH guidelines and global regulatory/import-export requirements
Partner with Quality on batch release, QP release for EU studies, deviations and change controls
Contribute to IND, IMPD and CTA regulatory submissions
Manage the clinical supply budget
Report to stakeholders and senior management on inventory, supply and demand, changes and risks

Requirements

What you’ll need

Bachelor’s or Master’s degree (or equivalent) in Life Sciences, Chemical Engineering or a related field
15+ years of progressive experience in clinical supply chain management, ideally with biologics, including significant experience leading teams
Proven experience managing clinical supply for biologics in vials within cold-chain environments, using local and multinational CMOs
Experience supporting multiple early- and late-stage programs, including multi-country Phase 3 studies and bridging studies for biologic combination products
Comprehensive understanding of global regulatory and import/export requirements across Europe, North America, China, Japan and Rest of World (ROW)
Strong working knowledge of cGMP, GDP and GCP
Hands-on experience with IRT/IxRS systems, clinical supply forecasting tools and budget management
Demonstrated success building and scaling clinical supply functions, including hiring, onboarding and managing team members and consultants
Exceptional communication, leadership and interpersonal skills
Strong problem-solving skills and ability to thrive in a complex, fast-paced clinical development environment

Benefits

Comp & perks

Remote work arrangement
Periodic travel to team and company events