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Current Experience

  • Scientist, Discovery Toxicology & Translational Safety Sciences, Preclinical Development & Safety

    Since May 2014

  • Scientist

    Since August 1997

Past Experience

  • In vitro Scientist, Safety Pharmacology Research, Translational Sciences, CREATe

    January 2012 --- April 2014

  • Scientist, Center of Excellence for Cardiovascular Safety Research & Mechanistic Pharmacology

    January 2008 --- January 2012

  • Scientist, Center of Excellence for Cardiovascular Safety Research, ion channel group

    April 2001 --- December 2007

  • Scientist, Electrophysiology, Department of Neuropsychopharmacology

    August 1997 --- March 2001

  • Research Assistant, Faculty of Medicine, Department of Physiology

    September 1992 --- July 1997


Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCollaborationEfficiencyFlexibilityOptimismResult OrientedResiliency


Self Assessment :
R&D Scientific writingAdverse Events (AE)Assay developmentBiologyBiomedical SciencesCardiologyCell Based AssaysCell CultureData AnalysisDrug DiscoveryDrug safety assessmentElectrophysiologyWriting Study Procedures and SOPsToxicologyStudy protocolsStem cell researchStem CellsScientific CommunicationsReport WritingPreclinical SafetyPre-clinical researchPhysiologypharmacologyPharmaceutical ResearchMedical writingLife SciencesIn Vitro
LinkedIn Assessment :
stem cell derived cardiomyocytescardiovascular safetyin vitro pharmacologyelectrophsiologyHigh Throughput ScreeningIon ChannelsCell CultureToxicologyIn VitroAssay developmentLangendorff heartHERGpatch clampDrug DiscoveryStem cell researchPharmaceutical IndustryLife SciencesFarmacologie, mens en dierPharmaceuticspharmacologyCell biologyBiotechnologyin Vitro Toxicology

Skills and Expertise

Self Assessment :
Analyze data Create SOPs Develop protocols Report data Write papers Write protocolsAttend seminars, courses and meetings within and outside the companyCell cultureConduct literature searchesConduct studiesControl studiesCreate SOPsCreate study documentsData verificationDesign scientific experimentsInterpret research resultsInterpret scientific datalifescienceManuscript preparation and reviewReview dataReview medical reportsSupervise techniciansWrite medical reports


  • Doctor of Philosophy (PhD) in Medical Sciences from KU Leuven in 1997
  • Ingenieur (Ir.) in Scheikunde en Landbouwindustrieën (Bio-engineer) from KU Leuven in 1992
  • GLP training for study directors, principal investigators, study staff and management in from BARQA, Cambridge in 0000


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    2 weeks
  • Positions I am interested in:
    Biomedical Scientist Clinical Data Reviewer Lab Scientist Medical Data Coordinator Medical translator Medical Writer Preclinical Scientist R&D Scientist Reviewer Scientific Researcher scientific translator Scientific Writer Scientist Senior Medical Writer Senior Scientist
  • Work From Home:
  • Work Regime:
    Permanent position :    60-100% FTE
  • International:

Area / Region



Driving License
  • Yes

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