Our Country Manager responsible for managing ClinTec’s Polish operations has over 15 years of experience in international clinical research and is a qualified Physician. She has experience overseeing clinical projects as Project Manager with the responsibility for organisational support and management of trials in Poland, Czech Republic, Slovakia and other CEE countries.

In her medical training, she specialised in Otolaryngology  and also has experience in other therapeutic areas including Gynaecology, Cardiology, Diabetes, and Oncology in Phase II-IV studies.  With considerable expertise in the area of Regulatory Affairs in Poland, she has worked as an EC and RA Submissions Specialist for 13 years, performing over 30 RA submissions and has been responsible for obtaining approvals for clinical studies from Phases II, III and IV.

Since joining ClinTec in 2004, she has been instrumental in expanding our Polish operations and now manages a large team of CRAs and CTAs in our Regional Office.

ClinTec's Regional Director for Central & Eastern Europe (CEE) and the Commonwealth of Independent States (CIS) spearheads our rapidly expanding team within this region. She is responsible for managing and developing ClinTec’s experienced team of Lead and Senior CRAs, Regulatory Associates and CTAs across Czech Republic, Slovakia, Russia, Ukraine and Balkan Region.

During 12 years in clinical research she was responsible for managing many complex global projects in Central and Eastern Europe from Phase I to Phase IV, across a number of therapeutic indications such as Urology, Gynecology, Endocrinology, Neurology and Oncology. She has a wealth of experience managing clinical trials in Czech Republic, Belgium, Romania, Bulgaria, Russia, Ukraine, Belarus and Uzbekistan.

With a perfect self-start and high achievement drive, she succesfully proved her ability to lead high profile initiatives within the business and manage multiple activities. She is a member of EFGCP and DIA and represents ClinTec in ACRO.