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Over the years I have gained a broad experience in clinical trials, thus becoming a truly all-round clinical research professional. I have managed all types of projects: from small phase 1 trials to large global, phase IIIB, full-service programs, as well as investigator initiated trials. I have worked in several indications, but mostly cardiovascular. Besides project- and line-management I have experience with many other aspects of clinical research such as: in-hospital trial coordination, site selection and start up, regulatory submissions, contracts & budgets, on-site monitoring, protocol & SOP development, database development, CRA training and coaching. Currently I 'm available for new projects, so if you need support on any task, please contact me on


Current Experience

  • Consultant Clinical Operations
    Since May 2014

  • Owner
    Since March 2014
    Clinical Research Consultancy

  • Project Manager
    Since May 2011
    Project Manager of multi-center, international, investigator initiated trials

Past Experience

  • Global Project Leader
    January 2007 --- April 2011

  • Head Clinical Research Coordination
    January 2000 --- January 2007


LinkedIn Assessment :
Clinical monitoringGCPCROCTMSClinical trialsPharmaceutical IndustryICH-GCPEDCTherapeutic AreasRegulatory submissionsClinical researchTrial ManagementClinical operationsClinical Data ManagementInfectious diseasesClinical DevelopmentPatient recruitmentPharmacovigilanceCardiologyProtocoloncology

Area / Region



Driving License
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