Director, Quantitative Clinical Pharmacology: PK/PD Modeling & Strategy

Role: Lead clinical pharmacology and pharmacometrics for Sarepta's drug development programs, including early to late-stage clinical trials (Ph3) and product registration. Responsibilities: develop and execute quantitative pharmacology strategies, oversee PK/PD modeling, population analyses, and translational studies; contribute to protocol design, data review, and regulatory interactions; serve as the functional lead for global regulatory strategies. Requirements: PhD in Pharmaceutical Sciences, Mathematics, Engineering, or related field; 7+ years in clinical pharmacology or pharmacometrics; expertise in PK/PD modeling, regulatory processes, and model-based analyses, with proficiency in NONMEM and R. Preferred: experience with siRNA, CNS, or mechanistic translational modeling. HighValue: emphasis on predictive modeling, regulatory engagement, global development, Ph3 trials, and product registration. WorkSetup: hybrid U.S.-based; on-site presence required; occasional in-person events.