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as rmm : medical monitor in global studies Phase II-iv (Neurology, immuno-oncology, hemato/oncology,urology, infection, ra, ibd ). 24/7 coverage

medical and operational oversight of studies in cee regon.

feasibility (program country Strategy, science)" >Protocol, site) - medical issues resolution ( medical oversight adding to scientific integrity, quality and safety aspects of studies)

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


Current Experience

  • Clinical Research Physician/RMM

    Since January 2012

    rmm at regional Clinical Development organization, pfizer czech republic,slovakia.

    RMM at Regional Clinical Development Organization, Pfizer Czech Republic,Slovakia.

  • Regional Medical Monitor

    Since June 2011

Past Experience

  • Clinical Research Associate (CRA)

    January 2007 --- June 2011

  • Product Manager

    January 2006 --- January 2007

  • Product Specialist/Product Manager

    January 2005 --- January 2006

  • Product Specialist

    January 2000 --- January 2005

  • Medical Sales Representative

    August 1998 --- December 1999

  • Radiologist

    January 1995 --- January 1998
    sonography,ct, double contrast examination,arteriography


LinkedIn Assessment :
Clinical researchClinical trialsoncologyNeurologyRheumatologyInfectious diseasesUrologyGastroenterologyHematology/Oncologymedical monitoringPatient SafetySAE ReconciliationDrug DevelopmentClinical DevelopmentGCPICH-GCPMedicineRegulatory affairsDermatologyCardiologyPharmaceutical IndustryCRO managementGood Clinical Practice (GCP)


  • MD in Medicine from Masarykova univerzita Lékařská fakulta in 1995
  • in from High school Znojmo in 1989

Training and Certification

  • MD in 1995 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
  • International:

Area / Region

Prague, Czech Republic


Driving License
  • Yes

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