Associate Director, Clinical Supply

Role: Associate Director, Clinical Supply, leading global clinical supply chain planning and execution for Liquidia's pulmonary hypertension programs across multiple regions.

Responsibilities:

• develop and implement supply strategies, demand forecasting, and inventory management
• oversee manufacturing, packaging, labeling, distribution, and depot operations
• manage vendor relationships including CMOs, IRT providers, and couriers
• ensure compliance with regulatory standards (FDA, EMA, etc.) and GxP
• support regulatory submissions and audits
• collaborate cross-functionally with Clinical Operations, CMC, Regulatory, and Quality teams
• manage budgets and resource planning

Requirements:

• Bachelors or higher in Life Sciences, Engineering, or related field
• 8+ years in clinical supply chain management supporting global Phase I-III trials
• experience with labeling, packaging, demand planning, and IRT systems
• strong knowledge of GxP, ICH guidelines, and international regulatory requirements
• excellent project management, analytical, and cross-functional collaboration skills

Preferred:

• biotech startup experience
• experience managing supply for biologics or novel modalities
• domestic/international travel (10-20%)

HighValue:

global clinical trial supply, pulmonary hypertension indications, biologics/modality, GxP compliance, cross-regional collaboration, vendor management, regulatory support, early to late-stage development.

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