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Experiences

Current Experience

  • Drug safety coordinator/scientist


    Since August 2014

Past Experience

  • Pharmacovigilance Officer

    March 2013 --- March 2014
    •to handle the transfer to gpv of spontaneously reported adverse drug reactions and Adverse Events from Clinical trials. •to contact Sales representatives, study monitors, and Health Care professionals to obtain information •to perform safety reporting to competent authorities, investigators, Ethics comities and license partners •to train local staff in spontaneous case reporting and Adverse Events reporting during Clinical trials and other organized data collection schemes •to ensure that the adequate number of follow-up attempts is done in order to comply with global SOP and local regulatory requirements •to complete bayer study list of approvals, studies progression,…

  • Post-doctorat en biologie cellulaire

    September 2011 --- February 2013
    - study of Biological and Clinical aspects of mesenchymal stromal cells

Knowledge

LinkedIn Assessment :
PharmacovigilanceArgus Safetymolecular biologyLifesciencesCancer ResearchClinical researchCell biology

Education

  • Docteur in Sciences Biomédicales from Université libre de Bruxelles in 2011
  • Master in Biologie moléculaire et médicale, biotechnologie from Université libre de Bruxelles in 2006
  • Bachelier in Chimie from Université libre de Bruxelles in 2004
  • in from Athénée Royal Jules Bara in 0000

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Professional Proficiency
Dutch
Elementary Proficiency

Area / Region

Brussels, Belgium

Others

Driving License
  • Yes

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