Remote Global Clinical Supply Strategy Lead

Elevar Therapeutics; United States; Remote; USD 150,000 - 185,000; Full time

Job summary

Elevar Therapeutics is seeking an Associate Director, Clinical Supply Chain to oversee end-to-end supply for global clinical trials from packaging to labeling and distribution. You will partner with clinical, regulatory, quality and CMC teams to ensure study materials are delivered on time and in compliance.

You will lead strategy, risk management, and coordination with IRT vendors, manufacturers, and sites, while managing budgets and ensuring quality processes across geographies.

Qualifications

• Bachelor’s degree in engineering or scientific field with 12 years’ experience in clinical supply.
• Knowledge of cGxP (GMP, GLP, GCP) and quality systems; IRT experience.
• Packaging and label CMO management experience.
• Effective written, verbal, and presentation communication skills.
• Demonstrate Elevar’s core values while working remotely.

Responsibilities

• Develop end-to-end clinical drug supply strategies for global studies.
• Forecast investigational product demand based on enrollment and country needs.
• Manage production, expiry, and inventory risks with internal and external partners.
• Coordinate with IRT vendors and systems for site and depot supplies.
• Contribute to shipping, storage, and disposal instructions in clinical manuals.
• Handle shipment requests, track deliveries, and ensure regulatory compliance.
• Represent clinical supply on cross-functional study teams and manage budgets.
• Manage acquisition, labeling, packaging, and management of comparators.
• Occasional work outside normal hours to support global network.

Skills

cGxP knowledge

IRT knowledge

Communication skills

Budget management

Education

Bachelor's degree in engineering or scientific field

Tools

IRT systems

Job description

Elevar Therapeutics is seeking an Associate Director, Clinical Supply Chain to oversee end-to-end supply for global clinical trials from packaging to labeling and distribution. You will partner with clinical, regulatory, quality and CMC teams to ensure study materials are delivered on time and in compliance.

You will lead strategy, risk management, and coordination with IRT vendors, manufacturers, and sites, while managing budgets and ensuring quality processes across geographies.