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Monitoring clinical studies phases I-IV Feasibility, set-up, initiation, monitoring and closure of clinical trials

Site management


Experience in therapeutic areas:

• Ophthalmology


• Cardiovascular

• Dermatology

• Endocrinology

• Inflammatory diseases

• Gastroenterology


Current Experience

  • Senior Clinical Research Associate

    Since August 2012

  • Senior Clinical Research Associate (outsourced via Chiltern)

    Since August 2012

Past Experience

  • Clinical Research Associate (CRA)

    October 2008 --- July 2012

  • Project Manager

    December 2005 --- September 2008


Self Assessment :
IndividualitySelf-confidenceIndependenceOptimismSociabilityAssertivenessCreative thinkingAdaptabilityInterest in knowledge


Self Assessment :
Cardiovascular diseasesDermatologyEndocrinology and metabolismGastroenterologyInfectious diseasesNeurologyOphthalmologyMedical oncology Phases of clinical development (phase I to IV)ICH GCP guidelinesClinical trial audits and inspectionsInformed Consent ProcessSafety trialsEfficacy trialsCRODiabetes
LinkedIn Assessment :
Clinical trialsCROICH-GCPClinical monitoringElectronic Data Capture (EDC) Clinical research


  • Master's degree in Biomedische wetenschappen (Biomedical Sciences) from KU Leuven in 2005

Area / Region

Perk, Belgium


Driving License
  • Yes

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