Dr. Vladislav Kurtev

Moving forward smoothly and powerfully. Continuously looking for efficiency and excellence in all processes. Rowing as my hobby is also an exceptional teacher of key strengths for my professional career. Just like rowing, the management of medicinal products requires the ideal stroke.

A question of perspective.

As an external expert I am quick to see optimisation potentials in internal processes. With an aptitude for analytical and crosslinked thinking I wish to support your strategic transformation processes and assist your continued efficiency and success.

Your projects are invariably carried out reliably, completely and on time, under adherence to all regulatory requirements and quality standards. 

My training

  • Study of genetics at the University of Vienna (M.Sc.)
  • Study of biochemistry at the University of Vienna (Ph.D.)
  • Postdoctoral scientist at Bio Molecular Therapeutics Medizinische F&E GmbH/Institute of Vascular Biology and Thrombosis Research, University of Vienna

My professional formation

Long-term experience in the areas of clinical trials, regulatory affairs and pharmacovigilance at leading pharmaceutical companies, including:

Richter Pharma AG

  • Head of Medical Affairs & Pharmacovigilance
  • EU-Qualified Person for Pharmacovigilance (EU-QPPV)

GlaxoSmithKline

  • Clinical Research Scientist & Project Leader Clinical Research
  • De-Centralised Study Manager for Global Clinical Operations