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Current Experience

  • Sr. ISS Coordinator

    Since December 2015

    start-up of Clinical trials specialist.

    ec and ra submissions.

    icf adaptations.

    contract negotiations.


    Start-up of Clinical trials specialist.

    EC and RA submissions.

    ICF adaptations.

    Contract negotiations.


Past Experience

  • Student Job

    May 2009 --- September 2015

    -hamal signature: samplingteam. staaltjes uitdelen aan klanten van supermarkten.

    -van genechten-biermans: productiemedewerker. kwaliteitscontrole dozenproductie.

    -ariel: poetsvrouw

    -hummbee: all-round medewerker. samenstellen orders, aanvullen online shop, aanpassen foto's.

    -euro archive: inputmedewerker. nakijken database en aanvullen.

    -carrefour: hulp slagerij.


Self Assessment :
Analytical thinkingCollaborationCommunicativeCuriosityAuthenticityEfficiencyIndependenceInterest in knowledgeKindnessOptimismOrganizationProblem solvingService orientedStrategic thinkingAssertiveness


Self Assessment :
Western BlottingPCRGood Clinical Practice (GCP)Good Manufacturing Practice (GMP)Clinical researchPhases of clinical development (phase I to IV)Search literature on clinical trialsSDS-PAGEFluorescence MicroscopyInterventional RadiologyPatentsScientific WritingSerious Adverse Event (SAE)ELISADNA extractionDiagnostic radiologyQuality Assurance (QA)ICH GCP guidelines
LinkedIn Assessment :
Impact MCMicrosoft OfficeRadiationRadiation SafetyICH-GCPResearchOptical MicroscopyQuality Control (QC)

Skills and Expertise

Self Assessment :
Conduct university research Work under specific instructions Interpret data Search literature on clinical trials Use a confocal microscopy Write papersClinical data collection


  • Master in Biomedical Sciences from UGent in 2015
  • Master in Biomedische wetenschappen / Biomedical sciences - Radiation Science from Universiteit Gent in 2015
  • Bachelor's degree in Biomedische wetenschappen / Biomedical sciences from Universiteit Gent in 2014

Training and Certification

  • GMP in 2014 Training
  • ICH GCP in 2015 Certification
  • Laboratory Animal Science in 0000 Certification
  • Profess Basic ICH GCP in 0000 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    5 weeks
  • Positions I am interested in:
    Clinical Research Associate (CRA) Biomedical Scientist Clinical Laboratory Technician Clinical Project Manager (CPM) Clinical Research Coordinator Clinical Trial Coordinator (CTC) Clinical Trial Specialist (CTS) Clinical Trial Manager (CTM) Clinical Trial consultant Field Clinical Research Specialist GMP Coordinator Junior Laboratory Technician Junior Scientist Lab Scientist Laboratory Engineer Laboratory Assistant Pharmacovigilance Assistant Preclinical Scientist Project Assistant Project Engineer QA Consultant QA Engineer QA Officer QC Specialist Regulatory Affairs Associate Regulatory and Start-Up Specialist RSU Specialist Scientist
  • Positions I am NOT interested in:
    Clinical Trial Assistant (CTA)
  • Locations I am interested in:
    Antwerp, Belgium Brussels, Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl employee :    100% FTE
  • International:

Area / Region

Antwerp, Belgium


Driving License
  • Yes

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