Eugenia Radkova has been working in OCT since 2013. She is responsible for providing expert review and advise on all matters related to scientific methodology and clinical study design, development of a full set of medical documents (study protocol, informed consent, Investigator’s Brochure, clinical study reports) for clinical studies in various fields of medicine. Eugenia has a solid expertise both in interventional I-IV phase studies and observational epidemiological studies and programs.
Eugenia graduated with honors from the Mechnikov St. Petersburg State Medical Academy and is a holder of a scholarship from the Russian Government and the St. Petersburg Governor. She holds a PhD in Medicine and has a strong educational and research experience in pharmacology and preventive medicine. During her work in academic sphere she has published more than 50 scientific papers and took part in research projects as a co-author and co-investigator under government contracts and Russian federal target programs.
Extensive research experience and knowledge in medicine and pharmacology allow Eugenia to successfully address all issues related to drug development and clinical trials conduct. She is a member of EMWA and AMWA professional associations. She improves her professional skills in medical and regulatory writing, biostatistics, methodology and design of clinical trials on a regular basis through training courses conducted by Russian regulatory organization Scientific Centre for Expertise of Medical Application Products and foreign educational institutions (Harvard Medical School, Stanford University and others).
Eugenia is involved in a training programme for OCT clinical staff and is an experienced speaker at various educational events organized by the Skolkovo Innovation Centre and conferences arranged by OCT which gather a wide range of healthcare professionals every year.