Composed of experienced leaders from across the health care system, the Strategic Advisory Panel helps set IVI research priorities, steers the research agenda in collaboration with scientific leadership, and provides guidance on ongoing research efforts. Panel members represent diverse perspectives from across the health care community, including academia, patient advocates, payers, providers, and the life sciences industry. Their role is to provide advice and ensure the credibility and rigor in the research and policy products, and to ensure all parties have a voice in IVI activities.
Chair and Vice-Chair
Samuel Nussbaum, MD
Chair, Strategic Advisory Panel
Samuel Nussbaum, MD
Dr. Nussbaum serves as a Strategic Consultant to EBG Advisors, consulting arm for Epstein Becker and Green, where he advises life science companies, health care systems, and provider organizations. He also serves as a Senior Advisor to Sandbox Industries, a health care venture fund.
From 2000 until 2016, Dr. Nussbaum served as Executive Vice President, Clinical Health Policy, and Chief Medical Officer for Anthem. In that role, he was the key spokesperson and policy advocate and oversaw clinical strategy and corporate medical and pharmacy policy.
During his tenure at Anthem, he was responsible for over $100B in annual health care expenditures through business units focused on care management, health improvement, and provider network contracting. Dr. Nussbaum was instrumental in developing contracting approaches that link hospital reimbursement to quality, safety and clinical performance; and patient-centered medical homes, assessing their impact on the quality and cost effectiveness of care. Under his leadership, HealthCore has built partnerships with Federal agencies and academic institutions to advance drug safety, comparative effectiveness and outcomes research.
Dr. Nussbaum currently serves on the Board of Directors of NEHI, America’s Agenda and PhyMed. He is a member of the Scientific Advisory Board of Medidata, the Healthcare Advisory Board of KPMG, the HHS Health Care Payment Learning and Action Network (LAN) Guiding Committee, Chairs the Innovation and Value Initiative (IVI) Board of Advisors, and participates in National Academy of Medicine initiatives.
Darius Lakdwalla, PhD
Vice-Chair, Strategic Advisory Panel
Darius Lakdawalla, PhD
Dr. Lakdawalla is the Chief Scientific Officer at Precision Health Economics and the Quintiles Chair in Pharmaceutical and Regulatory Innovation at the University of Southern California School of Pharmacy and Price School of Public Policy. He is the winner of numerous awards in health economics, including the Garfield Prize and the Milken Institute Distinguished Research Award. Dr. Lakdawalla is also a Research Associate at the National Bureau of Economic Research, and an Associate Editor at the Review of Economics and Statistics, the American Journal of Health Economics, and the Journal of Health Economics. Dr. Lakdawalla holds a PhD in economics from the University of Chicago, and a BA in Mathematics and Philosophy from Amherst College.
Dr. Lakdawalla also serves as the Executive Director of the IVI Strategic Advisory Panel.
Patient Advocate Foundation
Alan Balch, PhD
Dr. Balch has nearly fifteen years of executive leadership in the non-profit sector with an emphasis on consensus building and collaboration. He has led numerous federal advocacy efforts on a range of issues both that the legislative and regulatory level. He became the CEO of both the Patient Advocate Foundation (PAF) and National Patient Advocate Foundation (NPAF) in 2013. From 2006-2013, he served as the Vice President of the Preventive Health Partnership – a national health promotion collaboration between the American Cancer Society, American Diabetes Association, and American Heart Association. Prior to 2006, Dr. Balch was the Executive Director of Friends of Cancer Research.
Dr. Balch has served on the Executive Board of PAF and NPAF since 2007. He also serves on numerous advisory boards and committees.
He earned his PhD in environmental studies with a concentration in political economy from the University of California, Santa Cruz; master’s degree in environmental sciences in 1997 from the University of Texas in San Antonio; and bachelor’s degree (cum laude) in biology in 1994 from Trinity University in San Antonio.
Geisinger Health Plan
John Bulger, DO, MBA
John Bulger, DO, MBA, is the Chief Medical Officer for Geisinger Health Plan, Geisinger Indemnity Insurance Company, and Geisinger Quality Options, Incorporated. Dr. Bulger also serves as the Chief Medical Officer for Population Health at Geisinger Health System. In this key role, he works with Geisinger Health System and community providers to improve the quality of medical care for patients and members. Prior to joining Geisinger Health Plan, Dr. Bulger was the Chief Quality Officer at Geisinger Health System. He currently serves on various regional and national groups with the continued focus of striving to improve the quality of medical care. Dr. Bulger also chairs the Society of Hospital Medicine’s committee on healthcare quality and patient safety.
Randy Burkholder is the Vice President of Policy and Research at the Pharmaceutical Research and Manufacturers of America (PhRMA). Mr. Burkholder leads PhRMA work on policy solutions for supporting continued biopharmaceutical innovation and high-quality, patient-centered health care, including pavement and delivery reform, quality measurement, appropriate use and patient adherence, evidence-based medicine and health technology assessment, value of innovation and personalized medicine. Mr. Burkholder represents PhRMA at federal agencies and advisory bodies including the Medicare Evidence Development and Coverage Advisory Committee, CMS’ Technical Expert Panel on oncology, and the Federal Coordinating Council for Comparative Effectiveness Research. He is also a former member of the Board of Directors of the Personalized Medicine Coalition and serves on the Steering Committee of the Partnership to Improve Patient Care and the advisory committee for the Turning the Tide Against Cancer Initiative.
Mr. Burkholder has over 20 years of experience in health care policy, advocacy and communications in the medical technology and pharmaceutical industries. Prior to joining PhRMA, Mr. Burkholder was Associate Vice President for Public Affairs at AdvaMed, the leading association of the medical device and diagnostic industries.
American Express (Former)
Wayne N. Burton, MD
Wayne N. Burton, MD is Adjunct Professor of Occupational Medicine, University of Illinois at Chicago and Clinical Associate Professor of Medicine, Feinberg School of Medicine, Northwestern University. He was formerly the Chief Medical Officer for American Express and for JPMorgan Chase. He is Board Certified in Internal Medicine and a Fellow of the American College of Physicians and the American College of Occupational and Environmental Medicine. He has been the recipient of several awards including the Jonas Salk Leadership Award from the March of Dimes, the Health Leadership Award from the American College of Occupational and Environmental Medicine among others. He serves on several national advisory boards and on the editorial board of Population Health Management. Dr. Burton has published over 100 papers in peer reviewed medical journals.
National Pharmaceutical Council
Robert W. Dubois, MD, PhD
Robert W. Dubois, MD, PhD, is the Chief Science Officer and Executive Vice President of the National Pharmaceutical Council (NPC). In this role at NPC, he oversees the company’s research on policy issues as they relate to the role of real-world evidence in decision making, how to determine the value of health care services, the relationship between access and health outcomes, and the approaches to maintain an environment that supports health innovation. Dr. Dubois brings over 25 years of experience in health care research, with a key focus on understanding and ensuring that patients receive high value health care. Dr. Dubois is also a member of the Medicare Evidence Development and Coverage Advisory Committee, Advisory Board of the Institute for Clinical and Economic Review, the Associate Editor of the Journal of Comparative Effectiveness Research and on the editorial board for Health Affairs and The American Journal of Managed Care. He has published more than 150 peer-reviewed articles.
Biotechnology Innovation Organization
Daniel Durham, MPP
Daniel Durham is the Executive Vice President for Health Policy at the Biotechnology Innovation Organization (BIO) where he leads the development of policy positions promoting biomedical innovation and ensuring patient access to biopharmaceuticals. Previously, he held policy leadership positions at America’s Health Insurance Plans and the Pharmaceutical Research and Manufacturers of America. Mr. Durham also served as acting Deputy Assistant Secretary for Health Policy in ASPE at the U.S. Department of Health and Human Services and held key policy positions at the Social Security Administration, the Office of Management and Budget, AARP, and the California Legislative Analyst’s Office. He holds a Master’s degree in Public Policy from Duke University and a Bachelor’s degree in Government and Philosophy from the University of Notre Dame.
Patricia Fritz, MS
Patty Fritz is vice president, U.S. Corporate Affairs for UCB, Inc, overseeing policy, government affairs, advocacy, patient engagement, communications and UCBCares®. Patty leads efforts to create value for patients and their families through strategic engagement and positively influencing the healthcare environment and policy landscape. She is a champion of innovative projects to spotlight the importance of access and care for people living with severe diseases.
Having been with UCB for more than 20 years, Patty has made a significant impact in different leadership roles including Regulatory Affairs, Operational Excellence, Government Affairs and Policy. Patty led the regulatory efforts for UCB’s first product filing – Keppra® (levetiracetam) – and oversaw the FDA approval process for many of UCB’s other products.
Outside of UCB, Patty serves on the board of directors of Georgia BIO and The Carter Center Board of Councilors.
Patty holds a master’s degree in health care policy and administration from Mercer University, a Bachelor of Science degree in management and technology from the University of Maryland and is also a graduate of Summers County School of Nursing.
Jan Hansen, PhD
Jan Hansen, PhD, is Vice President of the Evidence for Access Unit within Genentech’s US Medical Affairs. Her unit is staffed with researchers who are uniquely positioned and skilled to address both the value and quality drivers of access in the US. These researchers are tasked to consider both value and quality evidence when they develop access strategies and tactics. Jan is a seasoned executive with more than twenty-five years of experience in the health care and pharmaceutical industries. Jan’s pharmacoeconomics and health outcomes expertise were acquired throughout her vast career experiences in patient-based research, health care consulting, sales strategy and execution, and in both global and US focused outcomes research. She has held positions with increasing leadership responsibility at several well-regarded companies, including PCS-Pharmaceutical Data Services (now CVS-Caremark), NDC Health, Wolters Kluwer Health, Glaxo Wellcome (now GlaxoSmithkline), and Allergan. Her professional accomplishments have been recognized by several professional organizations and resulted in numerous appointments, including: the University of Iowa College of Pharmacy Advisory Council, past Chair and current member of the University of Washington College of Pharmacy’s Corporate Advisory Council, Board member (representing Genentech) of the National Pharmaceutical Council (NPC), member of the Drug Information Association (DIA) Advisory Council of North America, past NPC Corresponding Officer and Research Committee member (representing Allergan), current member of the Academy Health Institution Council, and Foundation of Managed Care Pharmacy (FMCP) Board of Trustee. Jan is a licensed pharmacist and holds a Ph.D. in Pharmacy Administration from the University of South Carolina at Columbia. She is also a speaker and guest lecturer on topics related to pharmacoeconomics and outcomes research. Jan’s ultimate passion is “building”; she takes great pride in building organizations and fostering young, innovative-thinking, yet applied researchers. For Jan, there is no greater joy than watching these researchers flourish and making a difference to patients’ lives.
Kyle Hvidsten, MPH
Prior to joining Sanofi, Kyle worked at Vertex Pharmaceuticals where he served as the Head of Global Pricing and Reimbursement (formerly titled the Head of Global Market Access) and the Head of Global Health Economics. Prior to Vertex, Kyle held several roles at Pfizer. He holds a Master of Public Health degree from Columbia University and a Bachelor’s degree in Ecology from Emory University.
Sachin Kamal-Bahl, PhD
Sachin Kamal-Bahl, PhD, is Vice President and Head of the Global Health and Value Innovation Center at Pfizer, a newly created center under his leadership, that develops and integrates innovative approaches based on well-considered risks and strong technical underpinnings to address the access, pricing, or valuation challenges and opportunities facing the pharmaceutical industry. Under Sachin’s leadership and vision, the Center has been accelerating the pipeline of approaches to solve for the environmental challenges – examples of which range from leveraging joint EMA/HTA advice pathways, EMA adaptive licensing approaches, and systematic patient engagement in order to optimize drug development planning and access at launch to identifying innovative pricing and financing solutions for new drugs including those for curative treatments such as gene therapies in order to address payer concerns about prices and budget impact. Prior to coming to Pfizer in 2014, Sachin held various leadership positions in market access, pricing, and health economics and outcomes research at Merck & Co. In addition to leading the Innovation Center, Sachin holds adjunct appointments at two academic institutions, the University of Pennsylvania’s Leonard Davis Institute of Health Economics and the University of Maryland’s School of Pharmacy; serves on advisory boards of initiatives led by professional societies/organizations; and is a frequently invited speaker at external conferences.
Partners Healthcare System
Gregg S. Meyer, MD, MSc
Gregg S. Meyer, MD, MSc, is the Chief Clinical Officer of the Partners Healthcare System in Boston, Massachusetts, responsible for overall direction, operations, and management of system aspects of healthcare delivery throughout the Partners Healthcare delivery system. Dr Meyer previously served as the Chief Clinical Officer and Executive Vice-President for Population Health at Dartmouth-Hitchcock Medical Center, and held leadership positions at the Massachusetts General Hospital and Massachusetts General Physicians Organization (MGPO), the Agency for Healthcare Research and Quality (AHRQ), and Uniformed Services University of the Health Sciences (USUHS) where he served as a Colonel in the United States Air Force. He is a Phi Beta Kappa and summa cum laude graduate of Union College and magna cum laude graduate of Albany Medical College. He earned a Masters degree at Oxford University where he was a Rhodes Scholar. In addition, he holds a masters degree from the Department of Health Policy and Management from the Harvard School of Public Health and served as a fellow in the U.S. Senate Labor and Human Resources Committee’s health office.
Health Quality Advisors LLC
Michael L. Millenson
Michael L. Millenson, president of Health Quality Advisors LLC, is a nationally recognized expert on making care better, safer and more patient-centered. He is the author of the critically acclaimed book, Demanding Medical Excellence: Doctors and Accountability in the Information Age, and is an adjunct associate professor of medicine at Northwestern University’s Feinberg School of Medicine. He has testified before Congress and the Federal Trade Commission and written for publications ranging from The Washington Post to Health Affairs to the BMJ. He is a former board member of the Society for Participatory Medicine and serves on the editorial board of the American Journal of Medical Quality. Earlier in his career, as a healthcare reporter for the Chicago Tribune, he was nominated three times for a Pulitzer Prize.
Joshua Ofman, MD, MSHS
Joshua Ofman, MD, MSHS, is currently the Senior Vice President of Global Value, Access & Policy at Amgen. He received his advanced medical training in Gastroenterology from UCLA and his Health Services Research training from the RAND/UCLA/VA program. He formally was a member of the academic faculty in the Department of Medicine, UCLA School of Medicine, Cedars-Sinai Medical Center. Dr. Ofman also served as the Senior Vice President of Zynx Health Inc., a consulting company focused on evidence-based clinical information for quality improvement, and reimbursement and health economics strategy for life sciences companies.
Dr. Ofman currently represents Amgen on the Board of Directors of California Life Sciences Association (CLSA) and National Pharmaceutical Council (NPC).
Michael L. Ryan, PharmD
Prior to joining Bristol-Myers Squibb, Dr. Ryan spent 16 years at Amgen as the Vice President and General Manager for U.S. Reimbursement, Value and Access, where he was responsible for all pricing, contracting, government price reporting, payer strategy and value and access marketing across the $13B U.S. Amgen portfolio. He also served as the Vice President and General Manager of the Nephrology Business Unit for Amgen, where he was responsible for the P&L and life cycle management of Amgen’s three products used to treat patients with kidney disease; Epogen®, Aranesp®, and Sensipar®.
During his career, Dr. Ryan has been invited to present over 100 national platform presentations, and has over 30 refereed journal and textbook publications. The primary focus of Dr. Ryan’s research is pharmacoeconomics, pharmacoinformatics, healthcare policy, drug use and disease state management, and the application of Total Quality Management principals to a healthcare environment.
Dana Gelb Safran
Blue Cross Blue Shield of Massachusetts
Dana Gelb Safran, ScD
Dana Gelb Safran is Chief Performance Measurement and Improvement Officer and Senior Vice President, Enterprise Analytics at Blue Cross Blue Shield of Massachusetts (BCBSMA). In this role, she leads the company’s initiatives to measure and improve healthcare quality, safety and outcomes. Dr. Safran was among the lead developers of the BCBSMA Alternative Quality Contract (AQC), a provider contract model nationally recognized for pioneering payment reform and demonstrating significantly improved quality and cost. Dr. Safran retains an active academic practice, as a faculty member in the Department of Medicine, Tufts University School of Medicine, and has authored more than 80 peer-reviewed articles.
Harvard Pilgrim Health Care
Michael Sherman, MD
Dr. Michael Sherman serves as chief medical officer and senior vice president for Harvard Pilgrim Health Care. Dr. Sherman is responsible for Harvard Pilgrim’s medical trend management, provider engagement strategy, medical informatics, wellness and health promotion initiatives, care and disease management services, pharmacy services, NCQA accreditation and quality and utilization management programs and has been a leader in driving adoption of outcomes-based provider and pharmaceutical contracts. He also serves on the faculty of Harvard Medical School’s Department of Population Medicine, as chair of the Board of Managers of the Harvard Pilgrim Health Care Institute and on the Advisory Board of the Institute for Clinical and Economic Review (ICER). Dr. Sherman also is the current chair for AHIP’s CMO Leadership Council, comprised of chief medical officers from health plans throughout the United States.
Susan Shiff, PhD
Dr. Shiff joined Merck in 2014 as Senior Vice President and head of the CORE organization. CORE links together epidemiologists, health economists, access and reimbursement scientists, health services researchers and others involved in health policy research with the goal of leading global strategic value evidence generation and access strategy development to optimize reimbursement and patient outcomes across Merck’s portfolio. Prior to joining Merck, Dr. Shiff was the Global Vice President, Health Economics Research and Evidence Based Medicine at Teva, Inc. Prior to Teva, she spent seven years at Pfizer, including several years as Vice President in the areas of outcomes research, epidemiology, health economics, and access and pricing. She has also led the global risk management group and U.S. HEOR group at Roche and spent four years at the U.S. Centers for Disease Control and Prevention (CDC). In 2016, FiercePharma named Dr. Shiff one of the top 15 women in Biopharma. Susan received her Ph.D. from UCLA, and an MBA from Cornell University.
UPMC Health Plan
William Shrank, MD, MSHS
Dr. William Shrank joined UPMC’s Health Plan Division in June 2016 as the company’s new Chief Medical Officer. In this role, Dr. Shrank will focus on the design and implementation of new payment and delivery models to promote improved population health and further advance UPMC’s integrated clinical business strategies.
Prior to joining UPMC, Dr. Shrank served as Senior Vice President, Chief Scientific Officer and Chief Medical Officer of Provider Innovation for CVS Health where he led the development of solutions to support providers manage risk and deliver better care for the populations they serve. Prior to joining CVS, Dr. Shrank served as the inaugural Director, Research and Rapid-Cycle Evaluation for the Center for Medicare & Medicaid Innovation at the Centers for Medicare & Medicaid Services (CMS) where he helped design and led the evaluation of new payment reform models tested by the Center such as Pioneer ACOs, Bundled Payments and progressive Primary Care models. Dr. Shrank began his career as a practicing physician with Brigham Internal Medicine Associates at Brigham and Women’s Hospital in Boston, as well as an Assistant Professor at Harvard Medical School. His research at Harvard focused on improving the quality of prescribing and the use of chronic medications and he published over 200 papers on these topics.
Dr. Shrank received his Medical Degree from Cornell University Medical College, served his residency in Internal Medicine at Georgetown University and was a Fellow in Health Policy Research at UCLA, RAND. He earned his Master of Science degree in Health Services from the University of California at Los Angeles and his Bachelor’s Degree from Brown University.
Dr. Shrank has served on various national committees and advisory boards, such as the National Advisory Committee for FDA, CMS, White House (Networking Information, Technology Research and Development Program), DHHS and AHRQ. Among the many achievement awards Dr. Shrank received is the 2015 Healthcare Executive Transformation Award from the Los Angeles County Medical Association. He also was the recipient of the Robert Wood Johnson Pioneer Award to evaluate the effect of innovative prescription label design on adherence to chronic medication and health outcomes.
Vipan C. Sood, MBA
Vipan joined AbbVie in 2014 and is currently serving as Vice President, HEOR, Virology/EndoMetabolics/Neuroscience. Prior to joining AbbVie, he was Senior Director, Medical Affairs & HEOR for Mitsubishi Tanabe Pharma America, Inc. He also held positions at GSK & Sanofi, including Executive Director, HEOR at GSK and Senior Director, HEOR at Sanofi. Vipan has a degree in Pharmacy and also attended University of Illinois for his MBA.
MedStar Health Research Institute
Neil Weissman, MD
Neil Weissman, MD, is the President of MedStar Health Research Institute, the research organization providing scientific, regulatory and administrative support for research programs across the MedStar Health system. He is a professor of medicine at Georgetown University School of Medicine and directs the Cardiovascular Core Laboratories. Dr. Weissman has been recognized internationally as an expert in the use of cardiac ultrasound in multicenter trials. He is often invited to serve as an expert on panels and commissions for the U.S. Food and Drug Administration and the National Institutes of Health with over 200 peer-reviewed publications. Dr. Weissman has held multiple leadership positions throughout his professional career, including President of the American Society of Echocardiography and Governor of the American College of Cardiology.