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Jennifer Lannon
Vice President, Registries and Partnerships Patient-centered Outcomes Research @Alira Health
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WORK HISTORY
Vice President, Registries and Partnerships Patient-centered Outcomes Research @Alira Health
As Vice President of Registries and Partnerships at Alira Health, I lead the strategy, development, and commercialization of patient‑centered registries and real‑world data assets across multiple therapeutic areas. My work sits at the intersection of science, technology, and partnerships. I collaborate closely with non-profit organizations, academic leaders, and life sciences companies to design longitudinal registries, establish data governance and access models, and translate patient‑reported and real‑world data into actionable evidence for regulators, payers, and industry. I oversee end‑to‑end registry initiatives—from scientific committee formation and protocol development through contracting, data access frameworks, and sponsor engagement—ensuring that patient perspectives are meaningfully embedded into evidence generation. I am particularly passionate about advancing responsible, transparent use of patient data and building partnerships that generate real‑world evidence while delivering tangible value back to patient communities.
EDUCATION
Johns Hopkins Bloomberg School of Public Health
Pharmacoepidemiology and Drug Safety Certificate Program
Johns Hopkins Bloomberg School of Public Health
Master of Public Health - MPH, Epidemiology and Biostatistics
Patient Advocate Certification Board
BCPA (Board Certified Patient Advocate)
University of Maryland
Bachelor of Science (B.S.), Cell Biology and Genetics
ABOUT JENNIFER LANNON
Jennifer Lannon serves as Vice President of Registries and Partnerships at Alira Health, where she leads the strategy, development, and commercialization of patient‑centered registries and real‑world data assets across multiple therapeutic areas. Her work sits at the intersection of science, technology, and partnerships. She collaborates closely with patient advocacy organizations, academic leaders, and life sciences companies to design longitudinal registries, establish data governance and access models, and translate patient‑reported and real‑world data into actionable evidence for regulators, payers, and industry. She oversees end‑to‑end registry initiatives—from scientific committee formation and protocol development through contracting, data access frameworks, and sponsor engagement—ensuring that patient perspectives are meaningfully embedded into evidence generation. She is particularly passionate about advancing responsible, transparent use of patient data and building partnerships that generate real‑world evidence while delivering tangible value back to patient communities.Jennifer\'s career has consisted of 12+ years of experience as a program manager, partnership manager, and business developer. She has worked across patient-centered research, patient engagement and advocacy, and health innovation, including founding her own company to help women decide if, when, and where to freeze their eggs. She has been interviewed by the TODAY Show, Good Morning America, the New York Times, the BBC, the Washington Post, 60 Minutes, and others.Jennifer holds the Pharmacoepidemiology and Drug Safety Certificate from Johns Hopkins Bloomberg School of Public Health, the #1 epidemiology program in the United States. She is also a Master of Public Health candidate at Johns Hopkins Bloomberg School of Public Health. She holds her Bachelor of Science in Biology, with a concentration in Cell Biology and Genetics, from University of Maryland. She is a Board-Certified Patient Advocate.
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