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Current Experience

  • Regulatory Affairs Officer/Scientist Export
    Since April 2014
    OTC medicine: - Writing export dossiers M1, M2, M3 in eCTD structure - Respond to the evalution rounds of the authority of the concerned country - Control if mock-ups / packaging are compliant - Evaluating commercials - Communication with third parties

Past Experience

  • Clinical Research Coordinator (CRC) activities (partial)
    January 2014 --- April 2014
    - Scheduling drug intake of test subjects - Advising the test subjects about the study - Explaining the necesairy documents (informed consent,...) to subjects + signing

  • Clinical Trial Pharmacist
    September 2013 --- April 2014
    - Prepare clinical trial drugs - Quality control of clinical trial drugs - Writing procedures concerning the clinical pharmacy (how to prepare the experimental drugs)

  • Internship Pharmacist
    July 2012 --- January 2013
    - Advising patients - Preparing magistral preparations - Distribution - Controlling prescriptions

  • Student Job hospital pharmacy
    August 2011 --- August 2011
    - Magistral preparations - Checking prescriptions - Distribution


Self Assessment :
AssertivenessCollaborationKindnessTrustSociabilityOptimismInterest in knowledgeCuriosityAttention to detailCritical thinkingCreative thinkingProactivity


LinkedIn Assessment :
Pharmacy PracticepharmacologyPharmacovigilanceOrganic ChemistryPharmacotherapyPharmaceuticsClinical researchGCPGMPRegulatory affairseCTDRegulatory affairs export


  • Master of Science (M.Sc.) in Pharmaceutical Sciences from University of Antwerp in 2013
  • Bachelor of Science (B.Sc.) in Pharmaceutical Sciences from University of Antwerp in 2011
  • Secundair in Wetenschappen - Talen from Koninklijk Atheneum Mortsel in 2008

Training and Certification

  • Practical implementation of ICH GCP, European Directive 2001/20/EC in Clinical research in 2013 Training

Area / Region

Antwerpen, België


Driving License
  • Yes