"Join me, alongside experts from Novo Nordisk, Regeneron, George Clinical and Oximio on March 18th, 2025 at 15:00 UTC for the UNFOLD CT XChange panel on Opportunities VS Challenges for Patient Recruitment in EECCA, moderated by Diana Matiashvilli, Founder & CEO Paspigioni."
Vadym Kutsenok, Director, Country Site Activation Head for Ukraine and Hungary at IQVIA, graduated from the National Medical University with a Medical Doctor degree and a PhD in Oncology. He holds 2 patents, has authored 2 monographs, and has approximately 50 publications in medicine. He has received awards from the Presidium of the National Academy of Science of Ukraine. Vadym started his career as a Clinical Research Associate in clinical trials with IQVIA in 2006. Throughout his roles as Manager of Clinical Operations, Clinical Project Manager, and Regulatory and Startup Head, he gained invaluable experience in startups and monitoring clinical trials. His expertise is centered on providing high-quality service in compliance with local legislation and global clinical trial regulations. Vadym seeks creative solutions with a practical approach to problem-solving and aims to build long-term, professional relationships with clients and stakeholders.
"Join me, alongside experts from Novo Nordisk, Regeneron, George Clinical and Oximio on March 18th, 2025 at 15:00 UTC for the UNFOLD CT XChange panel on Opportunities VS Challenges for Patient Recruitment in EECCA, moderated by Diana Matiashvilli, Founder & CEO Paspigioni."
Vadym Kutsenok, Director, Country Site Activation Head for Ukraine and Hungary at IQVIA, graduated from the National Medical University with a Medical Doctor degree and a PhD in Oncology. He holds 2 patents, has authored 2 monographs, and has approximately 50 publications in medicine. He has received awards from the Presidium of the National Academy of Science of Ukraine. Vadym started his career as a Clinical Research Associate in clinical trials with IQVIA in 2006. Throughout his roles as Manager of Clinical Operations, Clinical Project Manager, and Regulatory and Startup Head, he gained invaluable experience in startups and monitoring clinical trials. His expertise is centered on providing high-quality service in compliance with local legislation and global clinical trial regulations. Vadym seeks creative solutions with a practical approach to problem-solving and aims to build long-term, professional relationships with clients and stakeholders.