Amrutha Baskaran serves as the Product Director at Vivli. She received a MD from Tbilisi State Medical University, Republic of Georgia and a master’s degree in Clinical Research from the Medical University of South Carolina (MUSC). In addition, she completed a Fellowship in Clinical Research Ethics from the South Carolina Clinical and Translational Institute at MUSC.
Prior to the current position Amrutha worked as a Clinical Trial Lead for a medical device company running clinical trials on aortic stent grafts. She has 6 years of clinical trials experience in both academia and industry setting. She has experience in various roles as the study lead, data manager and regulatory specialist which gave her the exposure of working on both national and global clinical trials. In the past, Amrutha served as an Institutional Review Board member at the University of California, San Diego and as an external reviewer for Clinical Research Ethics Consultation Services at MUSC.
Prior to joining Vivli, Elizabeth was an Architect at Insight, Inc., a Vivli development partner. At Insight, Elizabeth was one of the first developers for the Vivli platform, joining the project at its kickoff in 2017 and continuing to work on Vivli for much of the next 7 years. She played a key role in translating complex business requirements into an effective implementation, and became known as the development team’s domain expert. Her other Insight experience included a number of Azure-based projects in the healthcare and life sciences vertical, working as a full stack developer with design responsibility for numerous Web APIs. Prior to Insight, Elizabeth worked in the medical device industry, building native applications for computer-assisted medical devices, with responsibility for all application development, maintenance, and software-related regulatory support.
Catherine D’Arcy is the Associate Director of Operations for Vivli. Prior to joining Vivli, Catherine gained 30 years of experience in the pharmaceutical industry, most recently managing data sharing requests for GlaxoSmithKline, and prior to that within clinical trial operations. She has a bachelor degree in Medical Biochemistry from the University of London.
Rylie Garrison, MEd is the Grants and Finance Administrator of Vivli. She also serves as Senior Grants Administrator in the Division of Pharmacoepidemiology and Pharmacoeconomics at Brigham and Women’s Hospital. In this position, she oversees finance and compliance for approximately 150 research grants from a variety of federal and philanthropic sponsors. She received her MEd in Higher Education Administration in 2019.
Rebecca Li, PhD, is the CEO of Vivli and on faculty at the Center for Bioethics at the Harvard Medical School. Previous to her current role she was the Executive Director of the MRCT Center of Brigham and Women’s Hospital and Harvard for over 5 years and remains a Senior Advisor at the Center. She has over 25 years of experience spanning the entire drug development process with experience in Biotech, Pharma and CRO environments. She completed a Fellowship in 2013 in the Division of Medical Ethics at Harvard Medical School. She earned her PhD in Chemical and Biomolecular Engineering from Johns Hopkins University.
William is currently the Technical Operations Engineer. He joined the Vivli team in 2021.
He Holds a Bachelor of Science degree in Computer Science from UMass Lowell and a Bachelor of Arts degree in Criminal Justice from Plymouth State University. Before joining Vivli, William worked for the State of New Hampshire at the Department of Information Technology (DoIT), providing technical support to state employees.
Liz Graham serves as Senior Clinical Research Data Manager for Vivli. She received a Master of Public Health (MPH) from the University of New England and a Master of Data Science and Analytics (MS) from the University of Maryland. Additionally, she completed the Cross Cultural Health Immersion to Ghana, West Africa as part of a multidisciplinary team that evaluated integration of western health approaches with local medicine to improve cultural competence awareness.
Prior to this role, Liz coordinated multi-disease clinical trials at Johns Hopkins. She developed experience in oncological trial management, clinical EDCs, regulatory and protocol compliance standards. Liz is a member of the American Public Health Association and American Health Information Management Association.
Grace serves as the Communications and Digital Marketing Lead at Vivli. She develops Vivli’s organizational communication strategy in collaboration with senior leadership. She also manages the day-to-day implementation of that strategy, including creating website content, drafting marketing materials, and managing communications campaigns. She also assists with planning the Vivli Annual Meeting.
Prior to joining the Vivli team, Grace worked at the National Institutes of Health’s All of Us Research Program where she contributed to the program’s communication strategy for scientific audiences. She also has experience working for non-profits and mission-focused organizations, including the National Communication Association. She earned a PhD in communication at the University of Illinois at Urbana-Champaign in 2019.
Michael Stebbins is the President of Science Advisors, a science and health consulting firm he founded in 2018 to provide science, technology, and public policy guidance to private companies, philanthropies, and non-profit organizations. He previously served as the Vice President of Science and Technology for the Laura and John Arnold Foundation where he was responsible for identifying and pursuing opportunities for philanthropic investment in Science and Technology. While at the Arnold Foundation he led initiatives that opened public access to data and publications created in the course of federally funded scientific research, and championed efforts in scientific reproducibility. His work at the Foundation addressed a broad set of critical issues including FDA policy on transparency, improving organ donation rates, leveraging the intellectual property sitting on shelves of universities and Federal agencies as well as opening access to scientific research publications and data.
Dr. Stebbins served as the Assistant Director for Biotechnology in the Obama White House Office of Science and Technology Policy. At the White House, he developed eight Executive Orders and other directives addressing issues ranging from the antibiotic resistance crisis to restoring pollinator health. His work led to broad changes in practice across the Federal government regarding the purchasing of bio-based products, improving veterans’ mental health, increasing access to federally funded scientific research publications and data, improving scientific reproducibility, evaluating and addressing the preferential purchasing of antibiotic free meats, reforming the regulatory system for biotechnology products, and improving the management of scientific collections.
Dr. Stebbins previously served as a science advisor to the Obama Presidential Campaign and on the Obama White House Transition Team. He is the former director of biology policy for the Federation of American Scientists (FAS) where he led their biosecurity project. His work at FAS led to changes in how agents are trained to interact with scientists at the FBI Training Academy at Quantico. His team developed the first tools to train scientists on dual-use research of concern. He co-founded, and served on the board of directors for, Scientists and Engineers for America, and served as President of Scientists and Engineers for America Action Fund. In addition, Dr. Stebbins worked as a legislative fellow for U.S. Senator Harry Reid and a public policy fellow for the National Human Genome Research Institute. He is a former adjunct professor of bioethics at the University of Pennsylvania. Before coming to Washington, he was a senior editor at Nature Genetics.
Dr. Stebbins serves on the National Academies of Science Board of Research Data and Infrastructure. He received his B.S. in biology at SUNY Stony Brook and his Ph.D. in genetics while working at Cold Spring Harbor Laboratory.
Dr. Barbara Bierer is the faculty co-chair of the Multi-Regional Clinical Trials Center of Harvard and Brigham and Women’s Hospital (MRCT Center), a Professor of Medicine, Harvard Medical School and Brigham and Women’s Hospital, Boston and a hematologist/oncologist. She is the Director of the Regulatory Foundations, Ethics and the Law Program of the Harvard clinical and translational sciences center. Previously she served as senior vice president, research at the Brigham and Women’s Hospital for 11 years, and was the institutional official for human subjects and animal research, for biosafety and for research integrity. She initiated the Brigham Research Institute and the Innovation Hub (iHub), a focus for entrepreneurship and innovation.
In addition, she was the Founding Director of the Center for Faculty Development and Diversity at the BWH. In addition to her academic responsibilities, she serves on the Board of Directors of Public Responsibility in Medicine and Research (PRIM&R), dedicated to promoting the ethical conduct of biomedical and behavioral research; Management Sciences for Health (MSH), an international organization working in partnership globally to strengthen health care, local capability, and access; and the Edward P Evans Foundation, a foundation supporting biomedical research. Previously she has served as the chair of the Board of Directors of the Association for Accreditation of Human Research Protection Programs (AAHRPP) and as chair of the Secretary’s Advisory Committee on Human Research Protections, HHS. She has authored or co-authored over 180 publications and is on the editorial boards of a number of journals including Current Protocols of Immunology.
Dr. Bierer received a B.S. from Yale University and an M.D. from Harvard Medical School.
