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Current Experience

  • Clinical Research Associate (CRA)
    Since February 2014

Past Experience

  • Senior Clinical Research Associate
    May 2011 --- December 2013
    - Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH guidelines. - Performs investigative site file reconciliation; requests any new or updated site-related essential and non-essential documents and reviews them for content, consistency with other documents, and compliance with appropriate local regulatory requirements, ICH guidelines, project Standard Operating Procedures (SOPs), and sponsor requirements. - May serve as a resource for and interact with other functional areas to resolve site issues and facilitate project timelines

  • Clinical Research Associate (CRA)
    March 2008 --- May 2011

  • Clinical Trial Specialist
    December 2006 --- March 2008
    Conducts and facilitates the study specific start-up activities including selection and regulatory document collection; supports regulatory submissions, in-and external regulatory consultancy, performs EC submissions, informed consent customization and contract preparation.

  • International Regulatory Affairs Officer
    February 2005 --- December 2006
    Prepared and submitted registrations and variations file to International Competent Authorities in accordance with local regulations for hormonal medicinal products in the therapeutic areas of gynecology, fertility & obstetrics, men’s health.


  • Master and 3d cycle in Biomedical Sciences, General from Université de Liège in 2002
  • in from ILM in 0
  • in from Saint Jean Marie in 0
  • in from Saint Jean Marie in 0
  • in from Saint Jean Marie in 0

Area / Region

Braine le Château


Driving License
  • No