Elizabeth Dawn Flick
Director, Medical Evidence Generation @Ionis Pharmaceuticals, Inc.
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WORK HISTORY
Director, Medical Evidence Generation @Ionis Pharmaceuticals, Inc.
CA, US
Responsible for executing medical evidence strategy within the specialty and rare disease therapeutic areas. Role involves working closely with cross-functional teams including Medical Affairs, Clinical Development, HEOR, and Commercial teams to design and execute evidence generation activities that fill key data gaps identified in Integrated Evidence Plans, including design and conduct epidemiology studies/analyses, observational research studies, develop disease and product registries, and design and implement Phase 4 studies.
EDUCATION
University of the Sciences in Philadelphia
RPh, Pharmacy
Harvard T.H. Chan School of Public Health
ScD, Pharmacoepidemiology
University of California, Berkeley
MPH, Epidemiology/Biostatistics
Lycoming College
BA, Biology
ABOUT ELIZABETH DAWN FLICK
Pharmacoepidemiologist and pharmacist with experience in pharmaceutical industry roles spanning Medical Affairs (primarily), Clinical Development and HEOR. Specializes in clinical, patient-enrolling cohort studies (e.g, patient registries, Phase IV trials, post-marketing safety studies) primarily in oncology and hematology, and more recently, immunology and neurology. Skilled in leading large, cross-functional teams in planning and launching studies, developing and executing strategy, and creating and implementing Integrated Evidence Plans in collaboration with large, cross-functional teams. Tremendous expertise in study design, resource and budget management, study conduct and compliance, data review, statistical analyses, messaging and packaging of key data to health authorities and payors, and publishing of clinical data. Experienced at collaborating with internal and external stakeholders (e.g, functional leadership, Study Steering Committees, scientific collaborations), and in exploring novel approaches to extracting and analyzing clinical data from patient charts and electronic data capture systems, including exploring AI capabilities. Continually educates stakeholders on the value of medical evidence to enhance patient outcomes and management.Highly skilled in comparative effectiveness research, clinical data evaluation, and novel ways to increase the utility of RWD. Additional experience includes being a core member of teams that have developed and implemented Integrated Evidence Plans, have built an internal data lake, and have developed data governance and non-interventional research processes. Over a decade exploring automated EHR data extraction methods (most recently AI capabilities). Getting the right drug to the right patient at the right time is my personal and professional goal.
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