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Summary

Experiences

Current Experience

  • GCP/GLP Pharmacokineticist/Toxicokineticist


    Since March 2010
    • management and performance of toxicokinetic and pharmacokinetic analyses, interpretations and reporting, in accordance with the ocde glp and ich-gcp regulatory principles;
    • use and production of CDISC sdtm and adam compliant datasets;
    • review and advicing on pharmacokinetic Analysis planification and study designs;
    • development of budget and timelines.
    • Management and performance of toxicokinetic and pharmacokinetic analyses, interpretations and reporting, in accordance with the OCDE GLP and ICH-GCP regulatory principles;
    • Use and production of CDISC SDTM and ADaM compliant datasets;
    • Review and advicing on pharmacokinetic analysis planification and study designs;
    • Development of budget and timelines.

Past Experience

Knowledge

LinkedIn Assessment :
Life SciencesoncologyVascular BiologypharmacologyCell biologyPharmaceuticalsPharmacokineticsBiotechnologyIn VivoIn VitroEx VivoCell CultureCell Based AssaysWestern BlottingAnalytical ChemistryBioanalysisMass SpectrometryLC-MSGood Laboratory Practice (GLP)GCPData AnalysisLIMSSASCROClinical DevelopmentClinical researchToxicologyLifesciences

Education

  • PhD in Biomedical and Pharmaceutical Sciences (Oncology and Vascular Biology) from Université catholique de Louvain in 2008
  • Complementary Master in Pharmaceutical Sciences from Université catholique de Louvain in 2005
  • Master in Biomedical Sciences from Université de Liège in 2003

Languages

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

Work Preferences

  • Notice Period:
    13 weeks
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Publications

    Expert has 9 publications (Will be avalible with full profile)

Area / Region

Belgique

Others

Driving License
  • Yes

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