Associate Director, Clinical Supply

Scorpion Therapeutics; Morrisville (NC); On-site; USD 180,000 - 240,000; Full time

Job summary

Liquidia is seeking an Associate Director, Clinical Supply to lead global clinical supply chain planning and execution for pulmonary hypertension programs across regions. This role requires strong leadership in supply strategy, forecasting, and inventory management.

You will oversee manufacturing, packaging, labeling, distribution, and depot operations while managing CMOs, IRT providers, and couriers. Regulatory compliance and audits are key responsibilities in a fast-paced, cross-functional

Qualifications

• Bachelor's degree 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.

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.

Skills

Project management

Analytical

Cross-functional collaboration

Education

Bachelor's degree or higher in Life Sciences or Engineering

Tools

IRTs systems

Job description

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.