Global Clinical Supply Strategist

Liquidia Technologies; United States; On-site; USD 140,000 - 185,000; Full time

Job summary

Liquidia is seeking an Associate Director, Clinical Supply, to lead global clinical supply planning and forecasting across multiple countries. You will manage depot and site inventory, labeling and packaging oversight, and IRT/RTSM system setup, ensuring regulatory compliance and uninterrupted material availability for development programs.

The role requires 8+ years in clinical supply, strong cross‑functional leadership, and experience with CMOs and regulatory submissions.

Qualifications

• Bachelor’s degree or advanced degree in Life Sciences, Engineering, Supply Chain, or related field is required.
• 8+ years of progressive clinical supply experience across multiple countries and regions.
• Hands-on experience with global labeling/packaging strategies, IRT/RTSM systems, and vendor management.

Responsibilities

• Develop and execute global clinical supply planning and forecasting for multicountry studies.
• Lead material release, distribution, depot and site inventory management, and packaging oversight.
• Oversee IRT setup and maintenance, dating extension, and cold chain management.
• Ensure regulatory compliance with FDA/EMA/MHRA/PMDA and GxP standards.
• Manage CMOs, packaging vendors, depots, couriers, and IRT providers.
• Budget, resource planning, and cross‑functional coordination with Clinical Ops, Regulatory, QA, and Manufacturing.

Skills

Global clinical supply operations

Regulatory requirements

GxP & ICH guidelines

Project management

Cross-functional collaboration

Analytical thinking

Vendor & CMO management

Supply chain strategy

Problem solving

Entrepreneurial biotech mindset

Education

Bachelor’s degree or advanced degree in Life Sciences, Engineering, Supply Chain, or related field

Tools

IRT/RTSM systems

Job description

Liquidia is seeking an Associate Director, Clinical Supply, to lead global clinical supply planning and forecasting across multiple countries. You will manage depot and site inventory, labeling and packaging oversight, and IRT/RTSM system setup, ensuring regulatory compliance and uninterrupted material availability for development programs.

The role requires 8+ years in clinical supply, strong cross‑functional leadership, and experience with CMOs and regulatory submissions.