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Summary

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, …

Experiences

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

Knowledge

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 in 0000 Certification

Area / Region

La Louvière, Belgique

Others

Driving License
  • Yes

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