Director, Science
CurrentCo-lead transportability initiative by analyzing case studies, conducting literature reviews, publishing associated articles, and designing potential demonstration projects to help position Aetion as a leader in the real-world evidence spacePerform regulatory consulting for several high-profile pharmaceutical clients to demonstrate how real-world data can be used to address unique regulatory challenges (such as clinical trial futility and pregnancy safety surveillance) Drive strategic thought leadership on the role of real-world evidence in Medicare price negotiations by co-authoring related publications and pushing Aetion’s active engagement in policy-driven healthcare decision-makingAdvance understanding of the role of real-world evidence in health technology assessment policies for initial and reassessment scenarios so that clients and the research community at large better understand how to position such researchDevelop internal regulatory tools and scientific materials (e.g., Food and Drug Administrative guidance summaries, target trial emulation framework slides, etc.) to keep the organization abreast of current methodological and policy trendsSpearhead research into the effect of information bias on real-world data studies, supporting rigorous evidence standards for clients and strengthening Aetion’s credibility in understanding real-world evidence qualityContribute to the design of real-world data protocols for both descriptive (e.g., drug utilization and natural history) and comparative effectiveness studies
