New board member Dr Enrica Alteri spent 7 years in drug discovery and 5 years in clinical safety at Ciba-Geigy/Novartis and then went on to lead the Pharmacovigilance and Risk Management team at Serono in Geneva. In 2012 she joined the European Medicines Agency, where she held various senior positions and was a member of the Executive Board until 2020.
Ethics and Sustainability Board member
New board member Jeff Skopek is an Associate Professor of Law at the University of Cambridge and Deputy Director of its Centre for Law, Medicine and Life Sciences. His research explores the normative and conceptual foundations of health law, focusing in particular on controversies about what harms and benefits count.
Ethics and Sustainability Board member
The Ethics and Sustainability Board is chaired by Professor Marie-Claire Cordonier Segger, an international expert in sustainability, law and public policy. It was established by Prof Cordonier Segger in the early days of bit.bio. The board’s role is to review company strategy, from R&D and clinical translation to commercialisation and operations and provide guidance and recommendations as well as align it with UN sustainable development goals.
bit.bio CEO and founder
Jeffrey Skopek is an Associate Professor of Law at the University of Cambridge and Deputy Director of its Centre for Law, Medicine and Life Sciences. His research explores the normative and conceptual foundations of health law, focusing in particular on controversies about what harms and benefits count.
He has served on the Research Ethics Committee of the University of Cambridge’s School of Humanities and Social Sciences, the Animal Welfare Ethics Review Board of AstraZeneca, and the Health and Social Care Advisory Panel of the UK government's Centre for Digital Ethics.
Before joining the University of Cambridge, he was an Academic Fellow at Harvard Law School’s Petrie-Flom Centre for Health Law Policy, Biotechnology, and Bioethics. Prior to that, he served as a law clerk to Chief Judge Lynch of the United States Court of Appeals for the First Circuit. He holds an A.B. in History from Stanford University, a Ph.D. in the History and Philosophy of Science from the University of Cambridge, and a J.D. from Harvard Law School.
After completing her medical studies in Rome and a post-doctoral fellowship focused on cellular immunology at the National Cancer Institute in Bethesda (USA), Dr Alteri spent 7 years in drug discovery and 5 years in clinical safety at Ciba-Geigy/Novartis in Basel. She was involved in major projects that yielded important drugs such as Gleevec for myeloid leukaemia, Coartem for malaria and Reyataz for HIV-AIDS. In 1998 she joined Serono in Geneva where she led the Pharmacovigilance and Risk Management team. At Serono, Dr Alteri was instrumental in establishing the company’s pharmacovigilance processes, as well as implementing the entire portfolio’s safety risk management strategy.
In 2012 she joined the European Medicines Agency, where she was Head of the Safety and Efficacy Sector for one year, being later promoted to Head of the Human Medicines Evaluation Division, and then to Head of the Human Medicines R&D Support Division.
She was a member of the EMA Executive Board from 2013 until she retired in 2020. In these roles, Dr Alteri was part of many high impact EMA initiatives, from the transparency of clinical trial data to the development of regulatory science strategy to 2025.
Dr Alteri has been consulting for the Swiss regulatory agency (Swissmedic), and is currently a member of the Scientific Committee and faculty of the Master Course in Drug R&D of the University of Geneva. Dr Alteri regularly gives lectures on various aspects of R&D at the Universities of Rome, Cattolica and LUISS, and at the European Course in Pharmaceutical Medicine at the University of Basel. Moreover, she is member of the CIOMS Working Group XIII (Real World Data/Real World Evidence), and the CIOMS Working Group Education. Most recently, she has been appointed as Core Member of the Proposal Review Committee of Unitaid for a 3-year period.