Manager – Clinical Supply Chain

BeOne Medicines

. Manage drug supply activities for one or more clinical studies, including planning, label development, label and pack, and distribution .

Posted 11/6/2026full-timeRemote • United StatesSenior💰 $131,800 - $176,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical supply chain activities, including supply planning, GMP inventory management, and compliance with clinical study protocols. Proven ability to lead cross-functional projects, develop risk mitigation strategies, and ensure continuous patient supply while minimizing waste.

Highest-signal resume keywords

Clinical Supply Chain ManagementGMP Inventory ManagementIRT Systems ExperienceRisk Mitigation PlanningCross-Functional Project Leadership

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Supply PlanningProduction SchedulingLabel DevelopmentDrug AccountabilityCAPA ImplementationInventory ReportingClinical Study Protocol ComplianceStandard Operating Procedures CreationException InvestigationBulk Shipment Coordination

Certifications & Qualifications

Bachelor DegreeMaster Degree

Industry Keywords

BiotechPharmaceuticalCROCGMP EnvironmentClinical Supply Best Practices

About the role

Key responsibilities & impact

Manage drug supply activities for one or more clinical studies, including planning, label development, label and pack, and distribution
Develop and oversee supply plans to ensure continuous patient supply while reducing risk and minimizing waste
Represent Clinical Supply Chain on Clinical Study Teams and support internal stakeholders including Clinical Operations, Regulatory, Quality, and CMC
Align clinical demand requirements, supply plans, and timelines with Clinical Operations and study teams
Create supply and inventory plans and develop production schedules for clinical trial materials
Monitor production schedule adherence and make course corrections
Manage GMP inventory, inventory reports, upcoming expiry, and drug accountability
Manage label and pack CMOs and distribution vendors and oversee their daily activities
Investigate exceptions, determine root causes, implement CAPAs, and drive closure
Ensure label text and proofs comply with applicable rules, regulations, product specifications, and clinical study protocols
Coordinate stakeholder and CMO review and approval of labels
Support IRT user acceptance testing, develop IRT supply strategy, and oversee ongoing system supply activities
Coordinate and track bulk shipments to CMOs, depots, and vendors and maintain import licenses
Develop supply strategies, identify risks, and develop mitigation plans
Lead cross-functional drug supply projects and process improvements
Create and revise Standard Operating Procedures
Ensure supportive staff meet deliverables for successful study management

Requirements

What you’ll need

Bachelor or Master Degree in Business Administration, Operations Management, or similar education required
7+ years progressive experience in Clinical Supply Chain, preferably within the biotech, pharmaceutical, or CRO industry
Working knowledge of clinical supply best practices
Experience with IRT systems
Experience working within a cGMP environment
Knowledge of applicable rules, regulations, product specifications, and clinical study protocols
Ability to create supply and inventory plans and production schedules for clinical trial materials
Ability to manage GMP inventory and drug accountability
Ability to manage label and pack CMOs and distribution vendors
Ability to investigate exceptions, determine root causes, implement CAPAs, and drive closure
Ability to coordinate label review and approval
Ability to support IRT user acceptance testing and develop IRT supply strategy
Ability to coordinate and track bulk shipments and maintain import licenses
Ability to develop risk mitigation plans
Ability to lead cross-functional projects and process improvements
Ability to create and revise Standard Operating Procedures

Benefits

Comp & perks

Annual bonus plan eligibility for non-commercial roles
Incentive compensation plan eligibility for commercial roles
Discretionary equity awards
Employee Stock Purchase Plan
Medical insurance
Dental insurance
Vision insurance
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Wellness