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Motivated clinical data manager, looking for a new challenge in clinical research or pharmaceutical industry.


Current Experience

  • Clinical Data Manager (DM)
    Since May 2013
    - cleaning of the clinical data - SAE reconciliation - making of reports - participating in group meetings - parcitipating in medical review

Past Experience

  • PhD student
    October 2011 --- April 2013
    Fundamental research of the effect of iodine deficiency on the activation of the microvascularisation in thyroid cancer. - In vitro studies using thyroid cancer cell lines - In vivo studies using transgenic mice - techniques used: immunohistochemistry, Western blot, ELISA, RNA extraction, RT-PCR, ELISA, Laser-Doppler,..


BrightOwl Assessment :
DependabilityOrganizationWillingness to compromiseCuriosityPerspectiveApproachabilityImpulse commandAnger commandSelf-discipline
Self Assessment :
IndependenceEfficiencyAttention to detailOrganizationAdaptabilityInterest in knowledgeApproachabilityOptimism


BrightOwl Assessment :
Clinical researchClinical Data Management (CDM)Data entryMedical oncology Good Clinical Practice (GCP)
Self Assessment :
Medical oncology Clinical trial designRandomization and blindingDesigning case report formsData entryDatabase design and maintenancePrinciples and ethics of clinical researchPhase IIIGood Clinical Practice (GCP)Clinical researchLaboratoryMicrosoft OfficeIn VitroEnzyme-linked immunosorbent assay (ELISA)Immunohistochemistry (IHC)CancerClinical Data Management (CDM)PCR
LinkedIn Assessment :
Clinical Data Management (CDM)LaboratoryScientific WritingCRFSAE ReconciliationData Cleaning

Skills and Expertise

BrightOwl Assessment :
Ensure data consistencyManage clinical trial files/documentsDetermine statistical analysis Analyze dataClinical data collectionSerious Adverse Event (SAE) ReconciliationAssure medical quality Control data Report dataParticipate in medical review
Self Assessment :
Ensure consistency between the protocol and CRFInteract with physiciansInteract with statisticiansMaintain and manage internal clinical trial files and documentsWork collaboratively with the other members of the clinical research team


  • Master's degree in Biomedische wetenschappen (Biomedical Sciences) from Universiteit Antwerpen in 2011
  • Bachelor's degree in Biomedische wetenschappen (Biomedical Sciences) from Universiteit Antwerpen in 2009
  • secundair onderwijs in wetenschappen wiskunde from Sint Ursula Lyceum in 2006
  • secundair onderwijs in moderne from Sint Norbertus instituut in 2001

Training and Certification

  • Experimenter cat C (laboratory animal science and laboratory animal models) in 2010 Certification

Work Preferences

  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:

Area / Region



Driving License
  • Yes