Associate Director, Clinical Supplies

This role will support clinical priorities focused on quality, patient-centered outcomes, and effective care delivery. You will collaborate with clinical leaders, operational teams, and cross-functional stakeholders to improve standards, workflows, and execution. The position offers the opportunity to strengthen care quality, team performance, and measurable outcomes within a life sciences environment.

Location: Remote - US based candidates only, no visa sponsorship available

Responsibilities

• Lead CMOs, depots, and clinical supply vendors for investigational product management
• Partner with cross-functional teams to create clinical supply forecasts and study timelines
• Contribute to protocol development with a focus on investigational product logistics
• Author and maintain Pharmacy Manuals and Investigational Product Handling Manuals
• Train clinical sites and vendors on product handling and storage procedures
• Oversee the implementation and troubleshooting of IRT systems with external partners
• Monitor vendor performance and manage supply budgets and risk mitigation strategies

Requirements

• Bachelor's degree in biomedical, life science, supply chain, or related field required
• 8+ years of clinical supply chain experience within biotechnology, pharmaceutical, or CRO settings required
• Experience supporting global Phase I-IV clinical trials
• Experience managing external vendors, including CMOs, depots, and IRT providers

Benefits

• Premium health and financial offerings for employees and dependents
• Comprehensive wellness and employee support programs
• Life insurance and disability coverage
• Retirement plans with employer match
• Generous paid time off

Pay

$150,000 – $195,000 annually