We are dedicated to discovering novel biological targets and developing drugs that profoundly improve the lives of people born with rare metabolic defects who are unable to sustain basic biochemical processes necessary for life.
Our proprietary human disease models enable us to recreate and interpret complex human biology. We believe that no other company can match our ability to understand hepatic, tumor, or vascular diseases, and we value partnerships with other companies dedicated to accelerating novel therapies for challenging diseases.
HemoShear is more than our science and platform. We are a team of dedicated, innovative, and enthusiastic professionals that are passionate about our mission. Our values foster an environment in which we ask the tough questions and work collaboratively with urgency to discover breakthrough drugs to improve lives.
Prior to joining HemoShear in August 2008, Mr. Powers was a member of the executive team that took PRA International (now PRA Health Sciences) public in 2004. He transitioned PRA from a clinical data management company to a global clinical trials management organization, recruited its first operations leaders and led PRA’s business development activities. Mr. Powers served as an advisor to the UVA-Coulter Translational Research Partnership, which was funded by the Wallace H. Coulter Foundation. Mr. Powers was on the boards of CellzDirect and Averion during the time that both companies were successfully sold to larger R&D businesses. In 2014, Mr. Powers was selected to join PharmaVoice’s Top 100 most inspiring leaders in pharma. He currently serves on the board of Virginia BIO and is chairman of the Virginia BIO Foundation. Mr. Powers received a B.S. in administration and management science from Carnegie Mellon University.
Dr. Wamhoff co-invented the HemoShear technology and directed the successful development of human models of the vascular system, liver diseases and the tumor microenvironment. His efforts led to the launch of HemoShear’s proprietary drug discovery programs in rare metabolic diseases. Advancement of HemoShear’s REVEAL-TXTM platform has been achieved in part by Dr. Wamhoff’s role in securing significant NIH Small Business Innovation Research funding from five different NIH institutes. His passion and scientific vision have fueled the formation of productive partnerships with Takeda, Horizon and Carnot Biosciences. Dr. Wamhoff, former Associate Professor at the University of Virginia, has co-founded multiple medical device and therapeutics companies. He has authored or co-authored more than 70 papers and has been issued more than 10 patents. Dr. Wamhoff obtained a B.S. in biology with a minor in business administration from Rhodes College, where he was the 2011 Distinguished Alumnus; he received his Ph.D. in medical physiology from the University of Missouri.
Prior to joining HemoShear, Mr. Holsinger was Chief Financial Officer of education technology company Cricket Media, where he led the company through a public offering and ultimately returned to private status. Previously Mr. Holsinger held CFO and VP Finance positions with MCT, a cellular telecommunications provider in Russia and Central Asia; the Baltimore Stallions, a franchise in the Canadian Football League; and the Baltimore Orioles. Mr. Holsinger began his career with Arthur Andersen in Washington, DC and received his B.S. degree in accounting and management information systems from the University of Virginia.
Dr. Brian A. Johns joined HemoShear following a prolific 20-year career with GSK, where he co-invented Tivicay® (dolutegravir), one of the most widely prescribed antivirals on the market for HIV, currently being used by millions of patients worldwide. Dr. Johns is also co-inventor of the long acting injectable integrase inhibitor cabotegravir, currently under FDA review as a monthly HIV treatment. Dr. Johns spent the past four years working closely with Professor David Margolis as co-director of the UNC HIV Cure Center and Qura Therapeutics, a biotech partnership between ViiV Healthcare and UNC with the mission to find a cure for HIV. Along with his extensive experience from early discovery though phase 2 clinical development, Dr. Johns has authored or co-authored 50 peer reviewed journal articles and is an inventor on approximately 70 patent applications. He received a PhD in Organic Chemistry from Wayne State University and was an NIH Postdoctoral Fellow at the University of Virginia.
Dr. Gerry Cox is a board-certified clinical geneticist and pediatrician with nearly two decades of industry experience in leading clinical development programs for rare diseases. From 2016-2018, Dr. Cox was Chief Medical Officer at Editas Medicine, where he was a major contributor to the acceptance of the first IND for a CRISPR-based medicine delivered in vivo for a common cause of genetic blindness. Previously, he was Vice President of Rare Disease at Sanofi Genzyme, leading clinical development programs for several lysosomal storage disorders that resulted in approvals of therapies for mucopolysaccharidosis type I and II and Gaucher disease. He still sees patients at Boston Children’s Hospital, where he was previously on the full-time staff and completed his pediatrics and genetics training. He also is an instructor in pediatrics at Harvard Medical School. Dr. Cox received his MD, PhD from the University of California at San Diego and a BA in biology from Harvard College. He has over 75 peer-reviewed publications.
Dr. Hayes has more than 25 years of experience in research and development of innovative therapeutics for rare diseases and cancer. Through 2015, he was Senior Vice President of Regulatory Affairs and Pharmacovigilance at Synageva Biopharma prior to their acquisition by Alexion Pharmaceuticals, where he led efforts to support the approval of Kanuma for lysosomal acid lipase deficiency, and provided strategic regulatory leadership for additional rare disease pipeline products. Prior to Synageva, Dr. Hayes was Group Vice President of Regulatory Affairs at Genzyme, where over 11 years he led the regulatory function for oncology and biosurgery as well as CMC regulatory organization for all therapies. Prior to joining industry, Dr. Hayes served at FDA for over 9 years at the Center for Biologics Evaluation and Research, where he conducted independent research in cytokine biology and managed the review of numerous recombinant proteins. Dr. Hayes received a B.S. from Davidson College and holds a Ph.D. in immunology and experimental pathology from the University of Florida.
Prior to joining HemoShear in August 2008, Mr. Powers was a member of the executive team that took PRA International (now PRA Health Sciences) public in 2004. He transitioned PRA from a clinical data management company to a global clinical trials management organization, recruited its first operations leaders and led PRA’s business development activities. Mr. Powers served as an advisor to the UVA-Coulter Translational Research Partnership, which was funded by the Wallace H. Coulter Foundation. Mr. Powers was on the boards of CellzDirect and Averion during the time that both companies were successfully sold to larger R&D businesses. In 2014, Mr. Powers was selected to join PharmaVoice’s Top 100 most inspiring leaders in pharma. He currently serves on the board of Virginia BIO and is chairman of the Virginia BIO Foundation . Mr. Powers received a B.S. in administration and management science from Carnegie Mellon University.
Mr. Brooks is the CEO and President of NeuroBo Pharmaceuticals, Inc. and the Managing Director of Healthcare Capital LLC, which specializes in advising innovative, early-stage life sciences companies. Mr. Brooks is on the board of a number of for-profit and not-for-profit organizations, including Cellnovo (chair), Thermalin Diabetes (chair), Noxilizer, Hygieia, College Diabetes Network (chair) and Suffolk University. Mr. Brooks is the former President and CEO of the Joslin Diabetes Center, has co-founded seven life sciences companies and was co-founder of Prism Venture Partners, a $1.25B venture capital firm. Prior to that, Mr. Brooks was a senior executive at Pfizer and Arthur Andersen. He holds an M.S. in Business Administration and a B.B.A. from the University of Massachusetts at Amherst. He is a Certified Public Accountant.
Dr. Gould is President and CEO of Fulcrum Therapeutics, Inc., a privately financed drug discovery and development company with a focus on genetically defined diseases. Prior to Fulcrum, Dr. Gould was President and CEO of Epizyme, Inc., where he led the company through a successful public offering. From November 2006 to March 2010, Dr. Gould served as Director of Novel Therapeutics at the Broad Institute of MIT and Harvard. Previously, Dr. Gould was Vice President, Licensing and External Research at Merck Research Laboratories, where he held a variety of leadership positions during his 23-year tenure. Dr. Gould received a B.A. in chemistry from Spring Arbor College, a Ph.D. in biochemistry from the University of Iowa, and completed postdoctoral studies at Johns Hopkins University. Dr. Gould also serves on the boards of Fulcrum, Turnstone Biologics and Spring Arbor University.
Dr. Metters was previously president and CEO of Lycera Corp. and held a number of leadership positions over more than two decades at Merck & Co. Under her leadership Lycera developed a pipeline of immune modulator programs which led to an exclusive global collaboration with Celgene in 2015. Dr. Metters began her tenure at Merck & Co as a research scientist and progressed to become head of Worldwide Basic Research. During this time Dr Metters was integral to the discovery of the asthma drug Singulair® and subsequently chaired the Worldwide Business Strategy team for the respiratory business. Dr. Metters graduated with a BS in biochemistry from the University of Manchester Institute for Science and Technology and obtained her PhD from the Imperial College of Science and Technology. She is an author on more than 70 publications and has been listed on 29 patents. She also serves on the board of directors of Pharmaxis and scientific advisory boards of Bridge Medicines and Tri-Institutional Therapeutics Discovery Institute.
W. McIlwaine (Mac) Thompson, Jr. is a founding investor and a founding board member of HemoShear. He is of counsel to the law firm of Woods Rogers PLC and has represented companies in diverse fields including biotechnology, information technology, education and manufacturing. Mr. Thompson is on the board of directors and past chair of the UVA Curry School of Education Foundation and a member of the board of directors of Virginia Humanities. He has been on the board and past chair of the Community Investment Collaborate, a Charlottesville-based education and micro-finance organization. He is also a board member of a number of privately-held companies. Mr. Thompson graduated from Yale College in 1969 and the UVA Law School in 1972.
Mr. Watkins was President, CEO and a Director of Human Genome Sciences (HGS) from 2004 until the company was acquired by GlaxoSmithKline in 2012. During his tenure, HGS successfully developed and brought Benlysta to market, the first new lupus drug to be introduced in over 50 years. Prior to HGS, Mr. Watkins spent more than 20 years in senior roles at Abbott and its affiliates in the U.S. and Asia. During that time, he was President of TAP Pharmaceutical Products, Inc., where he led the growth from approximately $2 billion to over $4 billion in annual revenue. Previously, Mr. Watkins was a consultant with McKinsey and began his career with Arthur Andersen. He is former Chairman of the Biotechnology Industry Organization and continues to serve on its board. He is currently Chairman of the Board of Vanda Pharmaceuticals, Inc., and on the board of Horizon Pharma plc. He also serves on the board of Visitors of the College of William & Mary and the board of the Ann and Robert H. Lurie Children’s Hospital of Chicago. Mr. Watkins received his B.B.A. in accounting from William & Mary and his M.B.A. from the University of Chicago Graduate School of Business, now the Booth School of Business.
Mr. Woods is a founding investor and a founding board member of HemoShear. He was CEO of Butler International, where he led a successful corporate turnaround, public offering, listing on the NYSE, and eventual cash sale of the company managed by a major investment bank. He later co-founded a merger and acquisition consulting practice specializing in the insurance industry. His board affiliations include Scitent, Inc. and the University of Virginia Heart and Vascular Center. He was co-founder of the Keswick Community Foundation and has served on the board and executive committee of Habitat for Humanity of Greater Charlottesville. He earned B.S. and M.S. degrees in engineering and an M.B.A. from Cornell University.
Children's National Medical Center, Director Rare Disease Institute; Chief of Genetics and Metabolism; Margaret O’Malley Professor of Genetic Medicine; National Organization of Rare Diseases (NORD, Chairman of the Board)
King Faisal Specialist Hospital (KSA), Chairman of Medical Genetics
University of Zurich, Head of the Division of Metabolic Diseases at the Children's Hospital Zurich
Stanford University, Professor of Pediatrics (Genetics) at the Lucile Salter Packard Children's Hospital
University of Utah, Chief of the Division of Medical Genetics; Professor of Pediatrics at Primary Children’s Medical Center
Professor and Chair, Division of Gastroenterology, Hepatology and Nutrition, VCU; Chairman, NIH NASH Research Network.
President, BRG LLC; former VP Global Pricing, Reimbursement and Health Economics, Synageva BioPharma; Head of Pricing, Amgen; Senior Economist, RAND.
Former CMO, Editas; VP Clinical Development, Rare Diseases, Sanofi Genzyme
J Dillberger LLC; former Charles River Labs; Triangle Pharmaceuticals; Glaxo Wellcome
HayesWays LLC; former SVP Regulatory Affairs, Synageva BioPharma; Genzyme; FDA
President, Opti-Mol Consulting LLC; former Director of Chemistry, GSK
CEO of Life Biosciences; former Vice Chairman of PepsiCo, Inc.; President, Takeda Global Research and Development Center; Royal College of Physicians, London; American College of Endocrinology
Board Director, PureTech Health; former President, Pfizer R&D
Chief Scientific Officer at Ribometrix; former Head of R&D at HemoShear; CSO Cardioxyl; SVP Discovery Biology, GSK
Every day, we are working toward discovering new therapies to treat diseases and make a difference in people’s lives.
HemoShear provides a fast-paced, highly collaborative work environment. We offer our employees opportunities to advance knowledge that will lead to new drug discoveries. HemoShear seeks outstanding scientists and other professionals. If you are interested in joining a company that is changing the drug discovery and development paradigm, then contact us at email@example.com.
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