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Summary

monitoring clinical studies phases i-iv feasibility, set-up, initiation, monitoring and closure of Clinical trials

site management

audit

experience in Therapeutic Areas:

Ophthalmology

CNS

• cardiovascular

Dermatology

Endocrinology

• inflammatory diseases

Gastroenterology

Experiences

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

Personality

Self Assessment :
IndividualitySelf-confidenceIndependenceOptimismSociabilityAssertivenessCreative thinkingAdaptabilityInterest in knowledge

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

Education

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

Area / Region

Perk, Belgium

Others

Driving License
  • Yes

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