Education
- Doctor of Pharmacy (PharmD), Butler University
- Doctor of Philosophy (PhD), Clinical & Translational Science, University of Pittsburgh School of Medicine
- Master of Science (MS), Clinical Research, University of Pittsburgh
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Dr. Ruth Etzioni is a biostatistician who primarily focuses on cancer screening and early detection. Much of her work is in the area of prostate and breast cancer, where she develops methods for evaluating diagnostic tests; creates mathematical models to reflect the impact of screening tests on the incidence and mortality rates of these cancers; calculates costs and benefits of preventive screening; tracks population trends with regard to screening and related behaviors and works with investigators on trial design and analysis. Dr. Etzioni also researches overdiagnoses associated with certain screening tests — when screening finds cancers that would not cause symptoms or death within a patient’s natural lifetime. She also evaluates novel cancer biomarkers and tracks patterns and outcomes of cancer care. Dr. Etzioni leads the biostatistics core for the National Cancer Institute-funded multicenter Northwest Prostate Cancer Specialized Program of Research Excellence, or SPORE, and she has a longstanding interest in researching, tracking and working to eliminate health disparities.
Development and implementation of statistical methods for prostate cancer studies
Dr. Carolyn Rutter’s research interests include microsimulation modeling and model calibration, evaluation of diagnostic and screening tests, and meta-analysis and systematic reviews, with a focus on Bayesian approaches. She is interested in understanding and addressing health care inequities and assessing health care quality and provider performance. Dr. Rutter is a principal investigator for a Cancer Intervention and Surveillance Modeling Network (CISNET) team focused on colorectal cancer and led the development of the CRC-SPIN microsimulation model. Her CISNET work focuses on reducing the population burden of colorectal cancer by comparing the effectiveness of policies for CRC control. She is a fellow of the American Statistical Association and has published more than 150 articles in scientific journals. Dr. Rutter served as an affiliate member of Fred Hutch from 2012-2014. Previous to rejoining Fred Hutch, she worked as an investigator with Group Health Research Institute (now Kaiser Permanente Washington Health Research Institute), the UW Biostatistics & Health Services departments and RAND Corporation.
Dr. Rutter is a principal investigator (PI) for a Cancer Intervention and Surveillance Modeling Network (CISNET) team and led the development of the CRC-SPIN microsimulation model for colorectal cancer. She developed a likelihood-free method for model calibration, implemented using the R package “imabc”. This method is especially useful for complex models that are calibrated to multiple targets.
Rajshree Pandey, PhD, MPH
Dr. Rajshree Pandey specializes in evidence synthesis and comparative effectiveness research methods, including systematic reviews, meta-analyses, indirect treatment comparisons, and health technology assessments. Her research interests include application of these methods to develop impactful global HEOR strategies across therapeutic areas particularly rare diseases, with an emphasis on enhancing efficiency in HEOR using artificial intelligence and addressing health inequities in decision-making and advancing equity-focused research and collaboration. At CHOICE, she contributes to teaching and mentorship in evidence synthesis methods and HTA applications. Dr. Pandey holds a PhD in Health Sciences from the University of Delhi, India, and a Master of Public Health in Epidemiology from the University of Massachusetts Amherst, USA.
Dr. Parth Shah is a behavioral scientist and pharmacist who integrates these two disciplines to study and improve clinical practice and health policy in the delivery of cancer care. Dr. Shah’s research focuses on how pharmacies can be better used to provide cancer prevention and care services to their communities, such as HPV vaccinations for adolescents and colorectal cancer screenings for adults. His research interests also include medical and end-of-life decision-making and improving palliative care.
Courses taught:
Biography
Maria Agapova is an affiliate assistant professor in the Department of Pharmacy, she has helped teach the Medical Risk Analysis & Management course since 2013 and is a faculty advisor for Practicum. As a health economics and outcomes research medical affairs professional, Maria currently works at Gilead Sciences. She previously held similar roles at AbbVie and Teva Pharmaceuticals. Maria is also an affiliate faculty at the UW CHOICE Institute.
John Watkins, PharmD, MPH, BCPS managed the formulary process at Premera Blue Cross from 2000-2019. His responsibilities included health technology assessment, formulary process development, formulary reviews, and medical policy review and providing drug information support to medical and case management staff. He is currently Director of Premera’s PGY1 Managed Care Pharmacy Residency program and Student Advanced Pharmacy Practice Experience Coordinator. Along with these responsibilities, he manages the Pharmacy and Therapeutics Committee. John is Affiliate Professor of Pharmacy at the University of Washington. His areas of interest include health policy, health technology assessment and application of evidence-based medicine, personalized medicine, economics and bioethics to formulary and coverage decision making processes.
After graduating from the University of Washington (1979) and working as a community pharmacist, John served as a hospital pharmacy director pharmacology instructor for 7 years in Kathmandu, Nepal. He completed a combined MPH degree in Pharmacy and Health Services at the University of Washington (1993) with a residency at Group Health Cooperative, where he later worked as a clinical and drug information pharmacist. Before coming to Premera, he was a pharmacist at Regence BlueShield. He is board certified in pharmacotherapy, and has a PharmD, also from the University of Washington. He is a member of the AMCP Format Executive Committee, the ISPOR North American HTA Roundtable, HTA Council Working Group – Challenges in the Use of HTA in Pluralistic Healthcare Systems and the Precision Medicine SIG. He is a member of the Blue Cross Blue Shield Medical Advisory Panel.
John’s interest in formulary systems goes back to Nepal, where he established the first formal P&T committee and developed a combined formulary and drug procurement system serving 30 projects under two separate NGOs. It was there that he first became interested in the problem of managing scarce resources to maximize the value of pharmacotherapy at the patient level.
Dr. Roth specializes in comparative effectiveness research (CER) methods, including: observational study design, decision-analytic modeling, systematic review, meta-analysis, and generalized linear modeling. His research interests involve the application of CER methods to evaluate the benefit-risk tradeoffs and value of pharmaceutical and diagnostic technologies in cancer, with specific focus on pharmacogenomic testing applications, cancer screening strategies, and alternative treatment options in lung, breast, and prostate cancer. He received his MHA from the University of Washington Department of Health Services and a PhD in Pharmaceutical Outcomes Research and Policy from the University of Washington.
D.S. “Pete” Fullerton has had a distinguished career in managed care, teaching and research. From 1993-2003, he served as Vice President and Assistant Vice President for Regence Blue Shield, Seattle. In 2000, he received the Blue Cross Blue Shield Association’s highest award for innovative pharmacy programs.In 1998 he was one of the original developers of the drug dossier format which was later adopted by AMCP in 2000.In addition, he has been very active in the International Society for Pharmacoeconomics and Outcomes Research (ISPOR), and has served as a member of the Board of Directors.Dr. Fullerton’s academic background includes Professor of Pharmacy (affiliate) – University of Washington; Dean of Pharmacy, University of Utah; Associate Vice President and Professor of Pharmacy, Oregon State University.
Davene Wright, PhD is a member of the faculty at the Harvard Pilgrim Health Care Institute and Harvard Medical School. Dr. Wright received her doctorate in Health Policy and Decision Sciences from Harvard University. Her research aims to improve the supply of and demand for efficient health care that can improve the management of pediatric chronic diseases, with a focus on childhood obesity. In her work, she utilizes conjoint analysis, economic evaluation, simulation modeling, and health services research methods. Dr. Wright’s work has been funded by NIH, the American Heart Association, and the American Diabetes Association.
Prior to transitioning to her role at Harvard, Dr. Wright was an Acting Assistant Professor of Pediatrics at the University of Washington and an Investigator within the Center for Child Health, Behavior and Development at Seattle Children’s Hospital.
Dr. Steuten graduated with her MSc and PhD from the Department of Health Sciences at Maastricht University in Maastricht, NL. She is an associate member at the Fred Hutchinson Cancer Research Center and an affiliate associate professor in the Pharmaceutical Outcomes Research and Policy Program.
Dr. Steuten’s research expertise is in the fields of health economics and health services research. She specializes in developing and applying quantitative (Bayesian) methods for estimating and comparing the expected health and economic benefits of new approaches and interventions in cancer prevention and treatment, and prioritizing data collection to efficiently build the evidence for such promising new interventions.
Dr. Steuten’s research interests include developing and applying health economic and decision-analytic research methods to accelerate patient access to high value new screening, diagnostic and treatment options against cancer and other diseases.
Director of Education: Health Sciences BSc and MSc programs, University of Twente, Enschede, NL
Dr. Bansal is an Associate Professor and the Edwin S.H. Leong Chair in Data Science for Child Health at the Institute of Health Policy, Management and Evaluation, University of Toronto and The Hospital for Sick Children. Prior to joining the University of Toronto in September 2025, Dr. Bansal served on the faculty at The CHOICE Institute and Department of Pharmacy for 12 years. Dr. Bansal’s research focuses on sequential decision-making using longitudinal data, prediction modeling, decision theoretic methods including value of information analysis, and comparative effectiveness and outcomes research using large healthcare claims databases and EHR data. She is the PI of a study to develop methods for cost-effective personalized risk-adaptive surveillance in cancer.
https://www.ncbi.nlm.nih.gov/myncbi/aasthaa.bansal.1/bibliography/public/