medical and operational oversight of studies in cee regon.
trainings (medical) - visits and site interactions (oversight of clinical studies locally in order to provide high quality data )
review medical data, sae follow up
review science)" >Protocol,icf,crf.
lead rmm group medical monitors for coordination of mm activities within assigned clinical study.
previously: more than 12 years in the Pharmaceutical Industry in junior, middle level positions. held positions in Marketing & Sales in czech republic.then shifted to Clinical trials in hcr at vienna office, covering czech and slovak sites as CRA . cooperation with kol in different investigational sites. Negotiation and finalization up to signatures of contracts for Clinical trials. submissions to ec and ra. on-site and in-house monitoring of Phase II, iii, iv Clinical trials, conducting feasibility studies, authorization of Clinical trials and other drug Regulatory Affairs. specialties: therapeutic area experience: Neurology,infection,oncology,Hematology,hiv,icus,allergology,Dermatology,Psychiatry,Cardiology,urology,gastrology
Regional Medical Monitor
Since June 2011
Clinical Research Associate (CRA)January 2007 --- June 2011
Product ManagerJanuary 2006 --- January 2007
Product Specialist/Product ManagerJanuary 2005 --- January 2006
Product SpecialistJanuary 2000 --- January 2005
Medical Sales RepresentativeAugust 1998 --- December 1999
RadiologistJanuary 1995 --- January 1998
sonography,ct, double contrast examination,arteriography
MD in Medicine from Masarykova univerzita Lékařská fakulta in 1995
in from High school Znojmo in 1989
Training and Certification
MD in 1995 Certification