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Career path: -ph d in molecular biology, free University of brussels, belgium -three years of post doc experience at the University of chicago (molecular biology) -13 years of additional experience at the University of leuven belgium and vib with further acquisition of expertise in molecular biology, Cell-Cell Communication in embryonic development and disease (congential disease and tumor progression). -9 years of experience in pharma industry i.e. science writing (5 years, _immunotherapy in oncology) and Clinical safety and Pharmacovigilance (prophylactic Vaccines, 3 years), gcp and gvp, skills acquired on the job: -writing (grant Applications/Publications/Clinical documents e;g. Clinical study protocols and reports, Investigator brochures, informed consents, briefing documents, pbrers, Risk Management plans, dsurs etc) -Research: Assay development/ interpretation and dissemination of results -deep insight into molecular mechanisms of Gene transcription/Cell-Cell Communication/embryonic development/oncology/congenital disease -giving Presentations/Teaching/quick integration of information from literature -networking with experts both at level of University as at level of pharma industry -analytical and Critical Thinking -management: groupleader at University of leuven & vib/working within matrix structure in industry/interactions with external key stakeholders personal interests: continuous growth and learning engage in physical and emotional well being_physical activities few hours/week_course transactional Analysis


Current Experience

Past Experience


Self Assessment :
Cell biology Phase I R&D Scientific writingBiopharmaceuticalsBiotechnologyCancerCell CultureClinical DevelopmentClinical researchDNADNA extractionDNA sequencingDrug Safety and PharmacovigilanceDrug regulatory authoritiesDrug safety assessmentEarly development stageEnglishImmunologyInfectious diseasesInterpret clinical trial resultsKnowledge of the drug development processLaboratoryLaboratory study designMedical writingMicrosoft ExcelMicrosoft OfficeMolecular & Cellular Biologymolecular biologyMolecular CloningoncologyPCRPharmaceutical IndustryPharmacovigilancePhase IPhase IIPhases of clinical development (phase I to IV)ProtocolScientific methodologyScientific WritingSDS-PAGESerious Adverse Event (SAE)SOPVaccinesWestern BlottingInformed Consent DocumentsWriting Study Procedures and SOPs
LinkedIn Assessment :
embryonic development, cell-cell communication, gene expression, teachingmolecular biologyoncologyClinical trialsLife SciencesCell biologyCell CultureGeneticsBiotechnologyVaccinesBiochemistryGCPscienceCellPharmacovigilanceClinical DevelopmentAssay developmentImmunologyClinical researchPharmaceutical IndustryScientific Writing


  • Post doc in Molecular Biology from University of Chicago in 1991
  • Doctor of Philosophy (Ph.D.) in Molecular Biology from Free University of Brussels in 1987


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Work From Home:
    Yes, 0 to 5 days per week
  • International:

Area / Region

Tienen, België


Driving License
  • Yes

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