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Past Experience

  • In-house Clinical Research Associate/ Clinical Trial Associate Testelt, Scherpenheuvel-Zichem, Belgium
    April 2015 --- September 2015

    • Translation of clinical documents
    • Preparation of dossiers for submission to Ethics Committ
    • Preparation of Investigator Site Files
    • Performance of administrative tasks to support team members with Clinical trial execution: preparation and filing of clinical documentation

  • Clinical Research Associate (CRA) Brussels, Belgium
    June 2014 --- October 2014

    Indication: -Breast cancer: Phase IIIb, Belgium, 5 sites                      

                                                                          -mCRC: Phase IV, Belgium, 36 sites               

    Monitoring activities

  • Clinical Research Associate (CRA)/Study Coordinator Brussels, Belgium
    August 2013 --- March 2014

    • Clinical Research Associate                                  

    Indication: Viral Upper Respiratory Tract Infections Phase III, Belgium   

                 34 sites (General Practitioners)

    Responsibilities: Monitoring and Close-out visits   


    • Study Coordinator                                                                                                                                                  Indication: Hemato-Oncology: Phase IV, Belgium

    Responsibilities: Filling of CRFs

  • Clinical Research Associate(Trainee) Louvain-la-Neuve, Ottignies-Louvain-la-Neuve, Belgium
    February 2013 --- May 2013

    Indication: Viral Upper Respiratory Tract Infections

    Trainee Clinical Trial Associate role.

    Phase III, Belgium, 34 sites (General Practitioners)



    • Monitoring activities
    • Close-out visits


  • Clinical Research Fellow (Trainee) Seneffe, Belgium
    October 2012 --- December 2012

         ClinEt: Expert in Clinical Trials: Training                                                                                                                   

    - Planning and management of a clinical project

    - Regulatory aspects in use regarding human experimentation, Good Clinical Practice  

      and responsibilities of the CRA during his visits to physician investigators

    - Writing of scientific documents related to clinical trials

    - Proficiency in data management and in the functions of a Data Manager

    - Concepts in biostatistics for clinical trials and pharmaceutical research

    - Acquisition of the basic principles for an understanding of the pharmacovigilance

    - Knowledge and understanding of relationships between pharmacokinetics and  



  • Beauty consultant Brussels, Belgium
    February 2011 --- September 2012

    • Demonstration of the products
    • Sales of the products


  • Conduct a market study Brussels, Belgium
    September 2010 --- November 2010

    • Information retrieval on the internet and from bookstores
    • Development of a thesis



  • Quality Engineer Mont-Saint-Guibert, Belgium
    August 2007 --- May 2009

    • Management of Customer Quality Assurance department during the transition period
    • Participate in execution and implementation of a process on order returns during the launch of a company: Quality Assurance-Products distribution
    • Support of the interface between Fenwal and the logistic company
    • Take part in Quality meetings at customer sites
    • Coordination of complaint handling related to apheresis disposables and establishment of a new management process

  • QA Engineer Nivelles, Belgium
    October 1999 --- July 2007

    • Develop and coordinate communication channels between customers and plants
    • Take part in Quality meetings at customer sites
    • Support Sales functions, Marketing, Vigilance and Regulatory Affairs
    • Evaluate disposable complaints, preparation of reporting and trend analysis
    • CQA system trainer: Plasmapheresis system training
    • Control of the laboratory equipment and premises



Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCommunicativeCreative thinkingFlexibilityInterest in knowledgeProblem solvingResult Oriented


Self Assessment :
Medical devices R&DBiological Drug DevelopmentcGMPClinical researchCROCurrent Good Manufacturing Practice (CGMP)Data AnalysisDrug development processEnglishGood Clinical Practice (GCP)GMPKnowledge of the drug development processLogisticsMedical DevicesOncology Clinical ResearchPhase IIIProblem-solving methods and troubleshootingProject CoordinationQuality Assurance (QA)SAP

Skills and Expertise

Self Assessment :
Analytical skills Analyze dataCommunicate effectively on different company levelsCommunicationmanaging a small teamTeaching


  • Bachelor Medical biology in Biomedical Laboratory Techniques from Institut Paul Lambin in 2007

Training and Certification

  • ClinEt:Expert in Clinical Trial in 2012 Training
  • Junior CRA training program in 2007 Training
  • GMP training in 2004 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    Full Proficiency
    Professional Proficiency
    Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) QA Engineer QA Officer
  • Work From Home:
  • Work Regime:
    Permanent position :    80%-100% FTE
    BrightOwl freelancer :    40 Hours per week
    BrightOwl employee :    80%-100% FTE
  • International:

Area / Region

Brussels, Belgium


Driving License
  • Yes