Senior Director, Global Clinical Supply Chain (Remote)

BioAge Labs

United States

Remote

USD 210,000 - 230,000

Full time

5 days ago
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Benefits offered by this job

Remote work in the US
Competitive compensation package
401(k) with company match
Generous paid time off

Job summary

BioAge Labs is seeking a Director, Supply Chain (or Senior Director) for a fully remote role across the continental United States. You will lead the end-to-end clinical supply chain, collaborating with CMC, Clinical Operations, and external partners to ensure continuous availability of investigational products for global trials.

You will drive strategy, forecasting, vendor management, and budgeting while ensuring GxP compliance and timely material readiness across Phase 1–3 programs.

Qualifications

  • Experience leading end-to-end clinical supply chain for multiple programs.
  • Strong knowledge of GxP, GMP, GDP, ICH guidelines.
  • Proven ability to partner with Clinical Operations, Quality and Regulatory.

Responsibilities

  • Develop and lead clinical supply strategy for global trials.
  • Own end-to-end planning, forecasting, inventory, packaging, distribution.
  • Collaborate with cross-functional teams to align supply with milestones.
  • Lead vendor selection and management for CDMOs and logistics partners.
  • Establish KPIs for supply readiness and on-time delivery.

Skills

Leadership
End-to-end supply chain
Global clinical supply
Cross-functional collaboration

Education

Bachelor’s degree in related field
Advanced degree preferred

Tools

IRT/RTSM
ERP systems
Inventory planning systems

Job description

BioAge Labs is seeking a Director, Supply Chain (or Senior Director) for a fully remote role across the continental United States. You will lead the end-to-end clinical supply chain, collaborating with CMC, Clinical Operations, and external partners to ensure continuous availability of investigational products for global trials.

You will drive strategy, forecasting, vendor management, and budgeting while ensuring GxP compliance and timely material readiness across Phase 1–3 programs.

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