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. Responsibilities 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. Qualifications 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. Location & Salary 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. Benefits Includes a comprehensive benefits package covering physical and emotional wellness, financial wellness, and caregiver support. EEO Statement Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e‑Verify. #J-18808-Ljbffr