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This role involves providing scientific leadership for clinical development programs, supervising the clinical team, and ensuring compliance with regulations.

The Associate Director, Quantitative Clinical Pharmacology drives quantitative strategies and pharmacometrics analyses for drug development and regulatory strategies, requiring strong expertise in clinical pharmacology and PK/PD modeling.

The Senior Manager will lead global regulatory operations, ensure compliance in RIMS, and manage submissions to health authorities, improving processes and training users on RIMS.

Lead SOX compliance, technical accounting research, and documentation in R&D and manufacturing. Collaborate with leaders on financial impacts, ensuring compliance with U.S. GAAP.

The Senior Scientist will assess developability of lead biologic molecules through evaluation and characterization, collaborating across teams to define attributes and stability assays.

The Director will advocate for Sarepta's interests in state government affairs, managing relationships with officials, developing strategies, and ensuring compliance with state regulations while supporting the company's objectives in healthcare and legislative environments.