In 2021, COVAX’s efforts targeting long-term COVID-19 impact and beyond, transitioned into the “mRNA Technology Transfer Programme”, convened by WHO and its partner Medicines Patent Pool (MPP). Five Working Groups (WG) are responsible for the design and coordination of the activities required to fulfill the objectives of the mRNA Technology Transfer Programme.
A Scientific and Technical Advisory Committee (STAC) provides strategic, scientific, technical, and implementation-oriented advice to the mRNA Technology Transfer Programme Technical Leadership (WHO and MPP)
Additionally, a mRNA Scientific Advisory Committee (mSAC) convened by MPP comprising of experts in mRNA vaccine development provides technical input into the Programme.
The mRNA Technology Transfer Programme operates in close cooperation with the Biomanufacturing training initiative coordinated by WHO and the WHO Academy, to align training needs for both hub and partners (manufacturing, good practices, technology transfer) and training offer.
The Scientific and Technical Advisory Committee (STAC) provides strategic, scientific, technical, and implementation-oriented advice to the mRNA Technology Transfer Programme Technical Leadership (WHO and MPP) to support the realization of the vision of improving health and health security in low- and middle-income countries, and in particular pandemic preparedness, through sustainable, regional production of mRNA vaccines and therapeutics.
In its advisory capacity, the STAC may be requested to provide technical and strategic considerations in the following areas including, but not limited to:
Consortium partners contributing to mRNA technology development, industrialisation and transfer; and
Governance & Team » Governance Board
Chair of the Governance Board of the Medicines Patent Pool
Marie-Paule Kieny chairs the Governing Board of the Medicines Patent Pool Foundation (MPP, Geneva, Switzerland). She is also the Chair of the Board of the Drugs for Neglected Diseases Initiative (DNDi, Geneva, Switzerland) and a Non-Executive Independent Director of bioMérieux (Lyon, France). She is a member of the scientific advisory group of several organizations working in the area of health. Until May 2022, she was Director of Research at Inserm (Paris, France), a position where she chaired the French Scientific Committee on COVID-19 vaccine.
Until June 2017, Dr Kieny served as the Assistant Director-General for Health Systems and Innovation at the World Health Organization. Key successes under her leadership roles at WHO include coordinating the WHO R&D efforts during the 2014-2016 West-African Ebola epidemic and conceptualizing the WHO R&D Blueprint, a global preparedness plan against emerging diseases’ epidemics.
Before joining WHO, Dr. Kieny held top research positions in the public and private sectors in France.
Local Manufacturing Coordinator African Centers for Diseases Control and Prevention, Africa CDC
Abebe Genetu Bayih is the coordinator of local manufacturing of health commodities at Africa CDC. Prior to joining Africa CDC, he was the Africa Engagement Lead at Coalition for Epidemic Preparedness Innovations (CEPI). Abebe was also the Director General of the Armauer Hansen Research Institute (AHRI), Ethiopia for three years. AHRI is the biomedical and clinical research agency of the Ministry of Health of Ethiopia. In addition, Abebe was Associate Professor of Medical Parasitology at the University of Gondar, Ethiopia. He did his PhD on Molecular Microbiology at the University of Calgary, Canada. His PhD project was on vaccine discovery. He also did postdoctoral research on antimalarial drug discovery. Abebe is also a fellow of the London School of Hygiene and Tropical Medicine Global Health Leadership Programme.
Head of Department, Public Health Threats, European Medicines Agency (EMA)
Marco Cavaleri is Head of Department, Public Health Threats. He is the Chair of EMA Emergency Task Force (ETF) and responsible for EMA activities for emergent pathogens, vaccines, TB and AMR. He has been leading the EMA activities during the COVID-19 pandemic on vaccines and therapeutics. He leads EMA vaccines strategy and co-chairs the EMA vaccine confidence advisory group. He is also member of CEPI scientific advisory group.
He serves in different advisory groups at WHO, including PDVAC, R&D Blueprint TAG on prioritisation of therapeutics, TB vaccines TAG and Shigella vaccines TAG.
Marco Cavaleri is a Pharmacologist who spent several years in industry in R&D mainly in the area of anti-infectives covering different positions in preclinical and clinical development of new antibacterial, antitubercular and antifungal agents.
He has expertise in microbiology, animal models, vaccines, translational science and clinical trials.
He is co-author of several publications related to vaccines, infectious diseases and regulation of medicines.
Independent vaccine R&D expert with experience in vaccine development and manufacturing
Michel De Wilde has a long career in Vaccine Research and Development. He currently consults for the Vaccine Communiuty. From 2001 till June 2013, Michel De Wilde was Senior Vice President, Research & Development, at sanofi pasteur. While at sanofi pasteur, Michel drove the development and licensure by the FDA and other Regulatory bodies of a number of products. Sanofi Dengue vaccine was developed under his supervision. Michel was also instrumental in driving the acquisition of and defining the integration model for two biotech companies: Acambis and VaxDesign.
Michel has played a key role as a research scientist in the development of several new vaccines, most notably the recombinant Hepatitis B vaccine, as well as GSK’s Malaria vaccine candidate.
Acting Director of the Science and Innovation Directorate, Africa CDC
Dr. Mosoka Fallah is the Acting Director of the Science and Innovation Directorate at Africa CDC, where he is leading transformative efforts to strengthen health security and foster innovation across the African continent. With a distinguished career in global health and a passion for scientific advancement, Dr. Fallah is dedicated to reshaping Africa’s research and development (R&D) and clinical trial landscape through a strategic focus on financing, coordination and governance, and human capacity development. His vision centers on creating a sustainable research ecosystem in Africa, enabling the continent to independently produce medical products and address its unique health challenges. Dr. Fallah is championing robust clinical trials and research initiatives to bolster local manufacturing capabilities, ensuring self-reliance in medical product development. Collaboration is a cornerstone of his approach.
Africa Director of 1Day Sooner
Zacharia Kafuko is a molecular biochemist and an Arizona State University alumni of the Mandela Washington Fellowship. His work experience includes work as an academician in Clinical Chemistry.
At the start of the Covid-19 pandemic, he signed up as a prospective clinical trial volunteer for the Covid-19 challenge study. He is the Africa director of 1Day Sooner. His work focuses on global vaccine equity and the integration of developing countries into modern medical research.
1Day Africa (the African chapter of the international public health nonprofit 1Day Sooner) focuses on global health, vaccine equity and future pandemic preparedness through the enhancing of the African research capacity. The work promotes and supports medical and clinical studies on the African continent. 1Day Sooner leads campaigns in science, policy and ethics to stop the world’s most harmful infectious diseases.
Head of clinical immunology and allergy at the University of São Paulo School of Medicine (FMUSP)
Jorge Kalil is a physician scientist, Full Professor and Head of Clinical Immunology and Allergy at the University of São Paulo School of Medicine (FMUSP) and Coordinator of the Institute of Investigation in Immunology (iii), a Brazilian National Institute of Science and Technology (INCT). His scientific career focuses on immune recognition, tolerance, transplantation, autoimmunity, and vaccine development. He has led research programs on vaccines against Streptococcus, dengue, and COVID-19, including candidates that have progressed to advanced stages of development. He has authored more than 800 publications indeed in Web of Science and holds several patents. He was Director of the Butantan Institute from 2011 to 2017 and President of IUIS. Kalil is Member of the Brazilian Academy of Sciences and the National Academy of Medicine, Co-Director of the FOCIS Center of Excellence in São Paulo, and Director of a World Allergy Organization Center of Excellence. He holds a PhD in Immunology and Human Biology from the University of Paris, where he trained in the laboratory of Nobel Laureate Jean Dausset. He was an International Scholar at the Howard Hughes Medical Institute.
Professor of vaccinology and dean of the Faculty of Health Sciences at the University of the Witwatersrand (Wits), South Africa
Professor Shabir A. Madhi is Professor of Vaccinology and Dean of the Faculty of Health Sciences at the University of the Witwatersrand (Wits), South Africa, and Executive Director of the Wits Vaccines and Infectious Diseases Analytics Research Unit (VIDA). He is an internationally recognised clinician-scientist with three decades of experience in vaccine research, infectious diseases, clinical trials and global health, with a particular focus on generating and translating evidence relevant to low- and middle-income countries.
Professor Madhi has led and contributed to the development and evaluation of vaccines against major infectious diseases, including pneumococcal disease, influenza, respiratory syncytial virus (RSV) and COVID-19. His work encompasses early and late-stage clinical trials, vaccine effectiveness, epidemiology, implementation and health-policy research. He has extensive experience working across academia, industry, governments and international organisations to advance the development, evaluation and uptake of health technologies.
A central focus of his work has been addressing inequities in access to vaccines and other health technologies by ensuring that products are evaluated in populations and settings that are often underrepresented in global research and development. He has been closely involved in building sustainable clinical research and scientific capacity in Africa and in developing partnerships between African researchers and international academic and industry partners.
Executive Director of the A*STAR Infectious Diseases Labs (A*STAR IDL) and Executive Director at the Biomedical Research Council, A*STAR, Singapore
Lisa F.P. Ng is Executive Director of the A*STAR Infectious Diseases Labs (A*STAR IDL) and Executive Director at the Biomedical Research Council, A*STAR, Singapore. An internationally recognised infectious disease scientist, she has spent nearly three decades advancing research on emerging infectious diseases, including SARS, chikungunya, Zika, COVID-19, and Mpox. Her work has contributed to the development of diagnostics, vaccines, therapeutics, and critical insights into host-pathogen interactions. Prof Ng has played key leadership roles in Singapore’s pandemic preparedness and response efforts and actively contributes to international initiatives that strengthen global health security and outbreak readiness.
A Clarivate Highly Cited Researcher, Fellow of the Singapore National Academy of Science, and recipient of the President’s Science Award 2025, Singapore’s highest scientific honour, Prof Ng serves on numerous international scientific advisory boards and national government committees, helping to shape research, preparedness, and public health strategies globally.
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Programme Leader, CEPI
Martina Ochs is a microbiologist with extensive experience in vaccine development. She held positions with increasing responsibility in the vaccines division of the French multinational pharmaceutical company Sanofi where she worked on pre-clinical and early clinical stage vaccines against Tuberculosis, Otitis Media, Streptococcus pneumoniae, and Bordetella pertussis as well as combination vaccines.
Dr. Ochs joined CEPI in April 2022 and focuses now on RNA vaccine technology and viral pathogens with outbreak potential and support of CEPI’s 100 Day Mission.
Since 2023, Dr. Ochs serves on the Scientific Advisory Board of the EU-funded NOSEVAC project.
Independent senior advisor in the field of vaccinology University of Applied Sciences and Arts in Hannover
Nadia G. Tornieporth, MD, DTM&H acts as an independent senior advisor in the field of vaccinology and currently serves as interim Director, Clinical Development, at the Coalition for Epidemic Preparedness Innovations (CEPI). She is a member of the Board of Trustees of the Sabin Vaccine Institute and the Board of the Novo Nordisk Foundation Initiative for Vaccines and Immunity (NIVI) Development organization. During her academic tenure, Dr. Tornieporth served as Professor of Clinical Research and Pharmacovigilance at the University of Applied Sciences and Arts in Hannover, Germany.
Previously, Dr. Tornieporth led the Global Clinical Research and Development teams at Sanofi Pasteur and GlaxoSmithKline Biologicals. Over the course of her career, Dr. Tornieporth contributed to the successful licensure of more than 20 vaccines and holds clinical patents for malaria and dengue vaccines.
Chairman of Valneva (France)
Dr. Gerd Zettlmeissl has more than 40 years of R&D and General Management leadership experience in the biopharmaceutical industry. Since 2012 he served on the Board of Directors and Scientific Advisory Boards of a number of non-profit organizations and biotech/vaccine companies. He currently is the Chairman of Valneva (France) and a member of the Scientific Advisory Board of Biological E. (India).
Gerd Zettlmeissl is the former CEO of the vaccine biotech company Intercell (now Valneva). Prior to joining Intercell, he was Managing Director of Chiron-Behring (Germany) and held senior management roles in biopharmaceutical R&D and Technical Operations at Chiron (USA) and Behringwerke (Germany).
In 2010, he was named Vaccine Biotech CEO of the Year at the World Vaccine Congress. Gerd Zettlmeissl authored and coauthored a wide range of patents and publications.
The mRNA Scientific Advisory Committee (mSAC) is an independent committee convened by the Medicines Patent Pool (MPP) to deliver answers, on a consultative basis, to specific questions on scientific matters addressed to them relating to the mRNA Technology Transfer Programme.
Coordinator, Initiative for Vaccine Research at the World Health Organization (mSAC Chair)
Friede is the scientific officer responsible for vaccine delivery systems within the Initiative for Vaccine Research (IVR) at the World Health Organization in Geneva, Switzerland. In this position he is the WHO focal point for matters related to the development of technologies to improve vaccines including adjuvants, stabilization methods needle-free vaccine delivery systems.
Prior to joining WHO Dr Friede held several positions in the vaccine industry: He was Vice President of Development for Apovia Inc. a Californian vaccine development company, prior to which he was responsible for vaccine formulation and vaccine delivery research at Smithkline Beecham Biologicals (now GlaxoSmithKline). Martin Friede received his PhD in biochemistry from the University of Cape Town in South Africa.
Chief Science Officer & Global Head, External Scientific Affairs, Sanofi Vaccines
Danilo is Chief Science Officer and Global Head, External Scientific Affairs for Sanofi Vaccines since October 2021. He is responsible for external-facing functions of the Vaccines R&D unit, including teams for search-and-evaluation of vaccine candidates and vaccine innovations, scientific network development & partnerships, and external financing. He has over 25 years of experience in research and development of vaccines and biologics in both pharmaceutical and non-profit sectors. Prior to joining Sanofi in November 2017, he was the Chief Scientific Officer at Aeras, a non-profit vaccine R&D organization funded by the Bill and Melinda Gates Foundation. During his 19 years at the Merck Research Laboratories, Danilo contributed to the licensure of Merck’s human papillomavirus (HPV) vaccines, and the development of novel vaccine candidates and antibodies against multiple viral pathogens and novel immunotherapeutic approaches against cancer and neurodegenerative diseases. He also served on numerous advisory committees to the Bill & Melinda Gates Foundation Global Health Program, International AIDS Vaccine Initiative, NIH Integrated Preclinical/Clinical AIDS Vaccine Development Program, USAID Malaria Vaccine Development Program, and HIV Vaccine Enterprise. He received his Ph.D. degree in chemistry and post-doctoral training from the California Institute of Technology and the Scripps Research Institute-La Jolla, respectively.
Former Deputy Director of the Vaccine Research Center at the National Institutes of Health and the Chief of the Viral Pathogenesis Laboratory.
Dr. Graham is the former Deputy Director of the NIAID Vaccine Research Center and has developed novel vaccines and monoclonal antibodies for several viral diseases including the COVID-19 mRNA vaccine for which he has been widely recognized.
Barney S. Graham is an immunologist, virologist, and clinical trials physician with an extensive background in basic and translational research applied to vaccine development. He obtained an undergraduate degree from Rice University, a medical degree from the University of Kansas, and residency, ID fellowship, and PhD from Vanderbilt University where he was an R01-funded investigator before joining the NIAID Vaccine Research Center at NIH as a founding member in 2000. He retired as Deputy Director of the VRC in 2021 and is now an independent consultant and Senior Advisor for Global Health Equity at Morehouse School of Medicine in Atlanta.
He is an elected member of ASCI, AAP, and National Academy of Sciences. He is recipient of the Robert M. Chanock Award for lifetime contributions to RSV research, the Albert B. Sabin Gold Medal Award for contributions to vaccinology, the Albany Medical Center Prize in Medicine and Biomedical Research, and the National Academy of Sciences John J. Carty Award for the Advancement of Science. He was named one of the world’s 100 most influential individuals and one of the Heroes of the Year in 2021 by Time magazine and recognized as the Federal Employee of the Year by the Partnership for Public Service.
He is an author on more than 500 scientific publications, and a thought leader on emerging viral diseases and pandemic preparedness. He is best known for his research on RSV pathogenesis, structure-based vaccine design, and application of mRNA delivery technology. He was involved in the advanced evaluation of vaccines and monoclonal antibodies for HIV, Ebola, and Chikungunya, and developed novel vaccines for RSV, influenza, Zika, paramyxoviruses, and coronaviruses including the first COVID-19 vaccine and monoclonal antibody to enter clinical testing and that subsequently achieved Emergency Use Authorization and licensure.
MD, PhD, Co-Director, Penn Center for AIDS Research, Immunology Core Director of Vaccine Research, Infectious Diseases Division
Drew Weissman, M.D., Ph.D. is a professor of Medicine at the Perelman School of Medicine, University of Pennsylvania. He received his graduate degrees from Boston University School of Medicine. Dr. Weissman, in collaboration with Dr. Katalin Karikó, discovered the ability of modified nucleosides in RNA to suppress activation of innate immune sensors and increase the translation of mRNA containing certain modified nucleosides. The nucleoside-modified mRNA-lipid nanoparticle vaccine platform Dr. Weissman’s lab created is used in the first 2 approved COVID-19 vaccines by Pfizer/BioNTech and Moderna. They continue to develop other vaccines that induce potent antibody and T cell responses with mRNA–based vaccines. Dr. Weissman’s lab also develops methods to replace genetically deficient proteins, edit the genome, and specifically target cells and organs with mRNA-LNPs, including lung, heart, brain, CD4+ cells, all T cells, and bone marrow stem cells.
R3 Program Director at Wellcome Leap, global ARPA for Health, and Strategic Data Science Director at Toscana Life Sciences Foundation, Siena (Italy).
Duccio Medini leads the 60M$ RNA Readiness and Response program, co-funded by CEPI, to develop standardized, multi-product RNA manufacturing capabilities providing increased access to diverse biologics and sustainable pandemic response.
In executive roles of growing responsibility at Chiron, Novartis and GSK corporations, he led hundreds of data scientists in Vaccines R&D across Europe, US and Asia, holding Research Board, Innovation Board, Clinical Quality Board and Data Governance Board responsibilities.
Working across biological discovery, clinical development and public health, he discovered the pangenome concept co-founding the pangenomics discipline, contributed to the successful registration of four novel vaccines, including the first universal vaccine against serogroup B meningitis, led the Meningococcal Antigen Typing System (MATS) platform worldwide, developed transformative corporate data strategies, authored 50+ publications, books and patents in data science for health, population genomics and mathematical vaccinology.
Prof. Medini received his Ph.D. in Physics from the University of Perugia, Italy, with a residency at the Northeastern University in Boston, MA; is habilitated Full Professor of Molecular Biology; has served in international PhD school committees at the Perugia and Turin Universities in Italy; is honorary member of the Cuban Immunology Society, Fellow of the ISI Foundation, Strategic Board member of CINI’s Italian National Digital Health Lab; an IMD, ADVAC and UC Berkley alumnus.
Director, NIAID Integrated Research Facility (IRF-Frederick)
Dr. Connie Schmaljohn is the Director of the NIAID Integrated Research Facility (IRF-Frederick) where she provides overall scientific leadership to research activities and oversees collaborative research programs to advance medical countermeasures for highly pathogenic viruses. In addition, she serves as an expert consultant and advisor both nationally and internationally on the development of novel vaccine strategies for highly pathogenic viruses.
Dr. Schmaljohn earned a BS Degree in Microbiology from the University of Nebraska and a PhD in Virology from Colorado State University, after which she joined United States Army Medical Research Institute of Infectious Diseases (USAMRIID) as a National Research Council postdoctoral fellow. She continued her career at USAMRIID in multiple capacities culminating with a position as the Senior Research Scientist for Medical Defenses against Infectious Disease Threats for the US Army. Dr. Schmaljohn’s research background is in molecular virology and molecular vaccine development. She has served as President of the International Society of Hantaviruses, Chair of the American Society for Microbiology Biodefense Conference, and Chair of the International Committee on the Taxonomy of Viruses Bunyaviridae Study Group. She also has served on the Interagency Public Health Emergency Medical Countermeasure Enterprise (PHEMCE) Viral Hemorrhagic Fevers IPT, the Board of Scientific Counselors for the NIAID Vaccine Research Center, the Scientific Advisory Council for the Coalition of Emergency Preparedness Innovations (CEPI) and the Independent Product Group (IPG) for COVAX. She was elected to the American Academy of Microbiology (2007) and was selected as Fellow of the International Society for Vaccines (2015). She received the Order of Military Merit (2002), the Association of Military Surgeons of the United States Research Award (2002), the University of Nebraska Alumni Achievement Award (2012), and the Presidential Rank Award (2017). Dr. Schmaljohn has published more than 200 peer reviewed journal articles and reference works, has edited many books and special journal issues and holds numerous patent awards for vaccine development efforts.
Former director of chemistry at Moderna Founder of Antirna Inc
Suhaib Siddiqi is a scientist in the field of infectious diseases, nucleic acids and genomics. As a head of the departments, he led the research and development efforts at various biotechnology and pharmaceutical companies. He was the first director of chemistry at Moderna.
He has a doctorate in Chemistry from the University of Technology, Vienna, Austria. He currently serves as a scientific advisor to various biotechnology companies. He was inventor of a potent antiviral agent, (-)-5’-Noraristeromycin and Virtual Terminators for the DNA/RNA sequencing. He has published 31 peer-reviewed papers, and 47 patents.
Professor of Medicine, Department of Medicine Chulalongkorn University; and Scientific Chair of the Chula Vaccine Research Center
Kiat Ruxrungtham, MD, is a Professor of Medicine, Department of Medicine, Faculty of Medicine, Chulalongkorn University; and Scientific Chair of the Chula Vaccine Research Center (ChulaVRC); and Director of the Covid19 Vaccine Development Program, ChulaVRC. He is providing teaching and patient care on Allergy -Clinical Immunology and HIV Medicine at the King Chulalongkorn Memorial Hospital, Faculty of Medicine, Chulalongkorn University; and is mentoring junior researchers on HIV medicine, vaccine, immunology, and allergy research and also on clinical trials. He is currently leading the Chula-Covid19 mRNA vaccine development program. He has published more than 360 peer review papers on HIV, immunology, allergy, and vaccine.