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A part of my job includes: - Organising and attending internal meetings + providing reports - Support the Clinical team with administrative tasks - Follow-up of status of contracts - Filing / Archiving - Creation and review of presentations -.prepare submission to Belgian authorities - prepare submission to Ethics Committees - Submit to authorities and EC’s Submission through start-up: - prepare essential documents - send essential documents to sites - follow up return of documents - preparation of site master file, pharmacy file, patient file, …


Current Experience

  • Clinical Trial Assistant (CTA)
    Since April 2015

Past Experience

  • Secretary to the Clinical Research
    May 2011 --- April 2015

  • Secretary to the Ethics Committee
    May 2011 --- April 2015

  • Secretaire en Oncologie
    January 2011 --- May 2011


LinkedIn Assessment :
PowerPointRechercheMicrosoft WordMicrosoft ExcelHospitalsEnglishRecherche cliniqueMicrosoft OfficeResearchGCPOncologieHBonnes pratiques cliniquesAnglaisEssais cliniquesSecteur pharmaceutiqueServices de santSciences de la viePharmaceutical IndustryICH-GCPcomite d'ethiqueEthics CommitteeRecherche en oncologiePlanification de rsite initation visit

Training and Certification

  • Good Clinical Practice - GCP Certification

Area / Region

La Louvière, Belgique


Driving License
  • Yes