Kitty Ohel
About Kitty Ohel
Kitty Ohel is a Senior Regulatory Affairs Specialist at Novocure in Haifa, Israel, with over 14 years of experience in clinical trials and regulatory affairs.
Title at Novocure
Kitty Ohel serves as a Senior Regulatory Affairs Specialist at Novocure in the Haifa Area, Israel. In this role, she is responsible for ensuring that products comply with all regulations and standards relevant to the medical and pharmaceutical industry.
Experience at Regentis Biomaterials Ltd.
Kitty Ohel worked at Regentis Biomaterials Ltd. for a total of 8 years. She held the role of Clinical Trial Manager (CTM) from 2015 to 2019. Before that, from 2011 to 2015, she served as a Clinical Research Associate (CRA) in Israel. During this time, she was involved in overseeing and managing clinical trials to ensure their compliance and success.
Career in Clinical Trials Supervision and Coordination
Kitty Ohel has extensive experience in clinical trials, having worked in various roles across different companies. At Seraffix, she coordinated pre-clinical and clinical trials from 2010 to 2011. Prior to that, she supervised clinical trials at Nehora-photonics from 2008 to 2010. These roles have equipped her with in-depth knowledge and expertise in the field.
Educational Background and Qualifications
Kitty Ohel holds an M.Sc. in Microbiology and Immunology from Ben-Gurion University of the Negev, where she studied from 2003 to 2005. She also earned a B.Sc. (med. Sc) in Health Sciences from the same university, completing her studies between 2000 and 2003. This solid educational foundation has significantly contributed to her career in regulatory affairs and clinical trials.
Early Career Roles
Kitty Ohel began her career as a research assistant at Bio-Rap Technologies from 2005 to 2007. She then worked as a lab technician at Kamada for five months from 2007 to 2008. These early roles provided her with valuable hands-on experience in the medical and biotechnological research fields.