Associate Director, Clinical Supply Chain Engineer

Role Overview

Associate Director, Clinical Supply Chain Engineer – responsible for designing and developing a robust clinical supply chain that enables timely, compliant, and efficient delivery of investigational products worldwide.

• Participate in Clinical Trial Teams and Transition Teams to gather critical information to design and develop robust clinical drug supply operations.
• Analyze and improve end‑to‑end clinical supply chain processes, including packaging, labeling, distribution, returns, and reconciliation.
• Facilitate cross‑departmental meetings to ensure alignment, identify dependencies, and resolve integration challenges.
• Collaborate with functional leaders to harmonize processes, systems, and documentation for partnered & acquired assets.
• Partner with Manufacturing, Quality, Regulatory, and Clinical Operations to ensure clinical material availability aligns with study timelines and compliance requirements.
• Evaluate depot, site, and packaging network flows to optimize inventory positioning and shipment strategies, including temperature‑controlled and time‑sensitive materials.
• Lead continuous improvement initiatives focused on process standardization, error prevention, and operational scalability.
• Perform process mapping and evaluate capacity planning, workflow design, and continuous improvement using methodologies such as Lean or Six Sigma.
• Support investigations, root‑cause analysis, and corrective/preventive actions related to supply chain deviations or performance gaps.
• Manage projects with CMOs.

• BS in industrial engineering or equivalent with 10+ years of experience in a Pharmaceutical Operations organization and 3+ years of experience with clinical supply.
• Certification in Lean, Six Sigma, APICS/ASCM, or related disciplines.
• Experience with process optimization, data analysis, quality, and efficiency.
• Familiarity with GMP, GDP, and clinical trial supply requirements in regulated environments.
• Experience working with CROs, CMOs and third‑party vendors.
• Proficiency with quality systems including developing policies, SOPs, and work instructions.
• Excellent communication, problem‑solving, and cross‑functional collaboration skills.
• Ability to travel domestically and internationally.

This is a hybrid position. Expected to work on site at one of Sarepta’s facilities in the United States and/or attend company‑sponsored in‑person events.
Targeted salary range: $160,800 – $201,000 per year.

Includes a comprehensive benefits package covering physical and emotional wellness, financial wellness, and caregiver support.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e‑Verify.