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Questions of Ethics in Clinical Trials & The War in Ukraine – Part 1

Complimentary for DIA members, this global webinar series shares the clinical trial challenges in Ukraine and the region. Join us to create strategies for the future.

Presenters

Thalia  Arawi

Thalia Arawi

Founding Director, Salim El-Hoss Bioethics and Professionalism Program, American University of Beirut & Medical Center, Lebanon

Karla  Childers, MS

Karla Childers, MS

Head, Bioethics-Based Science and Technology Policy, Johnson & Johnson, United States

Karla Childers is Head, Bioethics-based Science & Technology Policy in the Johnson & Johnson Office of the Chief Medical Officer. Her primary responsibility is leading and coordinating various bioethics-based, science policy projects since 2013. Her longest running responsibility has been the support and coordination of J&J’s Clinical Trial Data Transparency Initiative. She is the Chair of the J&J Bioethics Committee and serves as a bioethics subject matter expert for internal and external policy work. Ms. Childers began her career in industry as a chemist and then project manager for global drug development teams. Ms. Childers is also the co-chair of the DIA Bioethics Community.

Francis P. Crawley, FFPM

Francis P. Crawley, FFPM

Executive Director, Good Clinical Practice Alliance - Europe (GCPA) (SIDCER), Belgium

Francis P. Crawley is the Executive Director of the Good Clinical Practice Alliance – Europe (GCPA) and the Strategic Initiative for Developing Capacity in Ethical Review (SIDCER) in Brussels, Belgium. He is a philosopher specialised in ethical, legal, and regulatory issues in health research, having taught at several European, Asian, and Middle East universities. He is an expert in ethical review, data protection, and data sharing. He is a Data Protection Officer (DPO) on European Commission funded clinical research programmes. He currently chairs the methodologies sub-group of the Real Word Data Working Group at the Faculty of Pharmaceutical Medicine, Royal Colleges of Physicians.

Viktoriia  Dobrova, DrSc, PharmD, PhD

Viktoriia Dobrova, DrSc, PharmD, PhD

Professor, Vice-chairperson, Research Ethics Committee of Clinical and, Diagnostics Centre, Ukraine

Viktoriia Dobrova is PhD (Medical Device) and Doctor of Science (Pharmacy), professor, and Vice-chair of the Research Ethics Committee of the Clinical and Diagnostics Centre of the National University of Pharmacy, Ukraine. She focused on studies in the fields of quality management and good statistics practice clinical trials, cost-effectiveness analysis, and research ethics. She took part in research ethics projects at international as well as national levels. She was involved in the development of regulatory guidelines, Master Degree Program “Clinical trials” for Clinical Research Professionals in Ukraine, and designed the curriculum and core courses for it. Now she is a Research Associate at Heidelberg University Hospital, Germany.

Ghaiath  Hussein

Ghaiath Hussein

Assistant Professor, Medical Ethics and Law , Trinity Biomedical Sciences Institute, Trinity College Dublin, Ireland

Chieko Ms. Kurihara

Chieko Ms. Kurihara

Specially-appointed Professor, Kanagawa Dental University, Japan

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