Primary Responsibilities Include:

• Supports and works collaboratively as well as independently with the Directors and RWE lead positions
• Supports retrospective and prospective study development, implementation, and interpretation
• Leads assessment, interpretation & communication of relevant scientific literature; maintains awareness of internal & external data resources & identifies appropriate studies for addressing questions of interest, independently performs data queries & summarizes epidemiologic information.
• Leads ad hoc scientific requests including targeted literature reviews, data analytics, and data interpretation
• Contributes to and/or reviews RWE content for study protocols, SAPs, study reports, slide decks, abstracts, posters, publications, and other presentations of scientific findings.
• Collaborates with other functional groups (e.g. Medical, Commercial, Regulatory Affairs) in preparing documentation for reimbursement agencies or other external organizations.
• Contributes to integration of RWE into the R&D clinical development process & post-marketing activities via participation in cross-functional clinical trial, clinical development, and global development teams, as well as RWE subteams.
• Maintains knowledge & skills on evolving epidemiological methods, tools & data sources.
• Supports safety epidemiology-related scientific work
• Performs other related duties as needed.

Desired Education and Skills:

• MSc. or Ph.D. or Sc.D. Epidemiology/Pharmacoepidemiology or MPH with experience in sources of real-world evidence and scientific research in the pharmaceutical industry.
• At least two years' experience in real world evidence research.
• Experience with rare disease and/ or muscular dystrophy is a plus.
• Ability to use or interpret results from data analysis or signaling software tools.
• Analytic skills for interpretation of RWE studies.
• Advanced competencies in data analysis in MS Excel, SAS or R. IHD experience a plus.
• Strategic risk management planning.
• Ability to work in a cross-functional team environment.
• Capable of problem-solving and creative thinking over a diverse scope of analytic and data related tasks.
• Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
• Candidates must be authorized to work in the U.S.
• Sarepta Therapeutics offers competitive compensation.
• Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.