8th Annual New England Life Sciences Panorama
March 12 @ 5:00 pm - 9:00 pm
The Life Sciences Panorama is back on March 12, 2020!
Since its inception eight years ago, Life Sciences Panorama (LSP) has grown strong and is now recognized by the life science community as an annual catalyst for knowledge exchange. This must-attend event will focus this year on Deconstructing the cost of Health Care – A roadmap to pricing, access and reimbursement for new therapies.
Panel 1: When do companies need a reimbursement strategy?
Jim is a serial entrepreneur with expertise in establishing and managing start-ups, including obtaining financing and developing core messaging and establishing key clients. Ability to seize on great ideas and develop business strategies to turn them into products, to attract and retain top industry talent, to understand and to effectively communicate complex technical ideas, to create and execute business plans, and to effectively execute on sales and marketing plans. Experience in multiple industries, including biotech drug development, consumer electronics, and audio electronics. Jim is currently Chief Business Officer at SynDevRx, Inc., a Cambridge company focusing on the link between cancer and metabolic hormone dysfunction.
Ms. Pitluck is the Head of Global Pricing & Reimbursement (P&R) at Spark Therapeutics, Inc., a fully integrated gene therapy company committed to meeting the needs of patients living with genetic diseases. In her current role, Ms. Pitluck priced the first US Food and Drug Administration-approved gene therapy for a genetic disease, LUXTURNA® (voretigene neparvovec-rzyl). She also led the roll-out of Spark’s unique alternate payment options and outcomes-based arrangements for LUXTURNA. She is now working to develop programs to help ensure timely patient access to future one-time gene therapies in development.
Prior to joining Spark, Ms. Pitluck was the Executive Director for Global P&R at Alexion Pharmaceuticals, leading all global P&R efforts, including dossier preparation and negotiations for Alexion globally. Ms. Pitluck was formerly the Director of Genentech’s Coverage & Reimbursement Policy and responsible for all US public payer policy and reimbursement issues for Genentech’s products. She also worked at healthcare consulting companies including Avalere Health and Covance Health Economics and Outcomes Services Inc., focusing on policy and reimbursement analyses for a variety of pharmaceutical, biotechnology, and medical device products related to care settings and disease areas. Ms. Pitluck received her Masters of Science at the London School of Economics and Political Science and her Bachelor of Arts from Washington University in St. Louis.
Michael Epstein is Head of Commercial Strategy at Ascenian Consulting, which specializes in evidence generation, positioning, pricing and value demonstration for health technologies. Mr Epstein helps Ascenian’s clients develop commercialization strategies that optimize access and uptake in the US, EU5 and Canada. Prior to Ascenian, Mr. Epstein was Principal in Global Market Access Consulting at Evidera, Director of Commercial Strategy and Reimbursement at United BioSource Corporation, and held specialized health technology commercialization consulting roles at Harris Interactive (now Nielsen), Roger Green and Associates, MedSpan and TVG. His research has been published in peer-reviewed journals such as J Ambulatory Paediatrics and has been presented at international conferences such as ECTRIMS. He has spoken at industry meetings such as CBI Forecasting for Personalized Medicines, and he has moderated payer panels at conferences such as ISPOR Europe. Mr Epstein holds an MS in public policy analysis, MA in political science, and BA magna cum laude in political science from the University of Rochester.
Before coming to Joslin, Dr. Herman spent nearly four years as Executive Director of the Group Insurance Commission (GIC), which provides and administers health insurance and other benefits to more than 450,000 employees and retirees of the Commonwealth, and their dependents. While there, Dr. Herman oversaw successful efforts to revamp the offerings of the GIC, created multiple new capabilities and efficiencies to improve interactions with GIC stakeholders and presented a strategic plan to optimize and grow the quasi-independent state agency.
Previous to her service at GIC, Dr. Herman was the Chief Medical Officer and then Chief Operating Officer for Harvard Pilgrim Health Care, one of New England’s largest non-profit managed health care organizations, providing care and coverage to more than one million members throughout Massachusetts, Maine and New Hampshire. Before that, she had been Chief of Internal Medicine at Harvard Community Health Plan’s Cambridge Center.
Prior to being selected as President and CEO, Dr. Herman served as a Trustee of Joslin Diabetes Center for six years. She has been a Clinical Instructor at Harvard Medical School with hospital appointments at Mount Auburn Hospital and Beth Israel Deaconess Medical Center and a guest lecturer at the Harvard School of Public Health. She also has been a Faculty Mentor in Brigham and Women’s Internal Medicine Residency.
Dr. Herman graduated from McGill University Medical School (Montreal, Canada). She completed her residency in Internal Medicine at the Royal Victoria Hospital (Montreal, Canada) and received a Master’s equivalent degree in Epidemiology and Biostatistics from McGill University while doing a fellowship year in Community Medicine.
Panel 2: Enabling Commercial success through payer-focused evidence development
Roman is an applied health economist and market access strategist at Certara, a company providing modeling & simulation, regulatory science, and scientific value assessment software and services to reduce clinical trial burden, accelerate regulatory approval and increase patient access to medicines. Roman’s role comprises the executive management of all strategic and scientific teams, and he actively participate in client engagements. As a market access strategist, he ensures that customers can leverage all of the benefits of our multidisciplinary team and integrated offer. Roman has personally led hundreds of engagements in the international market access and health economics and outcomes research context related to product value demonstration. He has deep experience in the management of multidisciplinary teams of scientific and strategic consultants across continents. Roman’s experience ranges from analytical activities such as economic modelling and database studies, to strategic activities such as developing product pricing and market access plans and communicating evidence internally and externally for our customers. He intervenes across the product lifecycle, including assessment of early phase assets, licensing due diligence, and go/no-go decision-making support, as well as launch planning and commercialization activities.Roman received both a Bachelor of Science degree in Mechanical and Aerospace Engineering and a Master of Engineering Degree in Mechanical Engineering and Engineering Decision Making from Cornell University
Peter J. Neumann, Sc.D., Director, Center for the Evaluation of Value and Risk in Health at Institute for Clinical Research and Health Policy Studies at Tuft Medical Center. Professor of Medecine, Tufts University School of Medicine
Peter J. Neumann, Sc.D., is Director of the Center for the Evaluation of Value and Risk in Health (CEVR) at the Institute for Clinical Research and Health Policy Studies at Tufts Medical Center, and Professor of Medicine at Tufts University School of Medicine. He is the founder and director of the Cost-Effectiveness Registry, a comprehensive database of cost-effectiveness analyses in health care. Dr. Neumann has written widely on the role of clinical and economic evidence in pharmaceutical decision making and on regulatory and reimbursement issues in health care. He served as co-chair of the 2nd Panel on Cost-Effectiveness in Health and Medicine. He is the author or co-author of over 250 papers in the medical literature, the author of Using Cost-Effectiveness Analysis to Improve Health Care (Oxford University Press, 2005) and co-editor of Cost-Effectiveness in Health and Medicine, 2nd Edition (Oxford University Press, 2016). Dr. Neumann has served as President of the International Society for Pharmacoeconomics and Outcomes Research (ISPOR). He is a member of the editorial advisory board of Health Affairs and the health policy advisory boards for the Congressional Budget Office. He has also held several policy positions in Washington, including Special Assistant to the Administrator at the Health Care Financing Administration. He received his doctorate in health policy and management from Harvard University.
John Tagliamonte has more than 20 years of experience in executive leadership with responsibility for corporate development, finance, commercial and business operations, strategic planning, finance and legal functions with established and emerging public and private life sciences companies. As the first Entrepreneur-in-Residence with the MassBio, he is responsible for forward-looking program content across the organization, while helping to develop the next generation of biotech entrepreneurs. He also serves on the business advisory boards of oncology drug startups WntRx and PercpTx. Previously he was Chief Business Officer of rare disease company Oxyrane and held various executive business leadership roles at Anchor Therapeutics, ImmunoGen and Johnson & Johnson, as well as venture investing with Safeguard Scientifics. He began his career as a scientist at Dana-Farber Cancer Institute followed by global business unit management at Bio-Rad. M. Tagliamonte received his M.B.A. from Boston College and his B.S. in molecular biology from Tufts University.
Early Bird until February 27, 2020:
About Life Sciences Panorama:
Life Science Panorama is an annual event organised by the French American Biotechnology Springboard and powered by FACCNE (the French American Chamber of Commerce of New England), a leading Chamber of Commerce in the US. Since starting the first edition of Life Science Panorama eight years ago, this event has grown strong and is now recognized by the life science community as an annual catalyst for knowledge exchange. This must-attend event addresses core topics of interest for companies at different stages of growth and offers fantastic networking opportunities for biopharma professionals.
About the French American Biotechnology Springboard (FABS):
The French-American Biotechnology Springboard (FABS) is a forum comprised of experienced French and American experts and leaders coming from Massachusetts-based biotechnology and pharmaceutical companies. The aim of the French-American Biotechnology Springboard (FABS) is to guide French Bio-Entrepreneurs in the highly-specific scientific, business, and cultural environment of New England.