Primary Responsibilities Include:

• Perform advanced quantitative pharmacology and pharmacometrics analyses and activities within assigned programs to yield high value PK/PD support for critical decisions and dose selection; interprets and presents results and recommends appropriate actions.
• Manage and develop translational and clinical pharmacology efforts such as study designs, protocol preparation, data analysis and reporting.
• Supports the development and execution of the quantitative pharmacology strategy of nonclinical and clinical development teams.
• Provide insightful regulatory strategy for clinical pharmacology and pharmacometrics support of drug filings and is responsible for the respective sections of regulatory documents.
• Develop and maintain strong knowledge of best regulatory practices, clinical pharmacology principles, PK/PD analysis methodology and drug development precedent.
• Develop and maintain scientific awareness and presence in the clinical pharmacology and pharmacometric discipline, publishes manuscripts and posters, presents at scientific conferences and other scientific forums.
• Perform other related duties as assigned.

Desired Education and Skills:

• PhD degree in Pharmacokinetics-Pharmacodynamics, Pharmacometrics, biomedical engineering, statistics, applied mathematics, or a related field with a minimum of 3 years of experience working as a clinical pharmacologist or pharmacometrician within pharmaceutical industry. A MSc degree with relevant experience is also considered with at least 5 years of relevant experience.
• Experience in developing advanced quantitative system in Pharmacometrics, PK/PD, PBPK models to aid in research and development decision making.
• Experience in ASO, GTx or rare diseases is a plus.
• Knowledge of Health Authority perspective on use of modeling and simulation.
• Excellent interpersonal, collaboration, English communication skills (both written and verbal).
• Strong analytical skills and strategic thinking.
• Proven ability to successfully manage projects and timelines, organize/track complex information, prioritize accordingly, and the ability to quickly adjust to shifting priorities and demanding timelines when necessary.
• Self-motivated with strong work ethic and the ability to work independently and efficiently.
• Experience working with stakeholders/partners at all levels, globally, across the organization.

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This position is remote. However, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

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