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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, 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 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.

  • 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