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Current Experience

  • Senior Scientist
    Since July 2013

Past Experience

  • Scientist
    March 2011 --- July 2013


Self Assessment :
CommunicativeEfficiencyOptimismOrganizationResiliencyResponsibilityResult OrientedStrategic thinkingTrustCompetitiveness


Self Assessment :
Animal models Negotiation R&DAnimal HealthBiotechnologyBusiness DevelopmentCell CultureCellular Product DevelopmentcGMPCharacterizationClinical DevelopmentClinical Study DesignClinical researchClinical study reportsCommunication SkillsData AnalysisDeveloping Clinical Trial ProtocolsEMAFDAGenomicsGMPGood Laboratory Practice (GLP)Good Manufacturing Practice (GMP)Grant WritingGrant PreparationIMPDINDInformed Consent DocumentsMarketing Authorisation Application (MAA)Microsoft OfficeNew Drug Application (NDA)New Business DevelopmentPhases of clinical development (phase I to IV)Potency assaysPreclinical developmentPresentation SkillsProduct developmentProteomicsQuality Control (QC)Quality Assurance (QA)Regulatory affairsStem cell researchStem CellsTeam ManagementTime ManagementVeterinary Medicine

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Analyze data Create SOPs Search literature on clinical trials Write papers Write protocolsAttend investigator meetingbudgeting of R&D activitiesCell culturecollaborate in research projects at universitiesCollaborate with principal investigatorCommunicate with investigatorCommunicate effectively on different company levelsCommunicate with sponsorCommunicationCoordinate ethics committeeCoordinate projectsCoordinate regular advisory boardCoordinate with the ethics commiteecoordinating research projectsCoordinationCreate SOPsCreates a collaborative team environmentDesign clinical trialDesign clinical presentationDesign protocolDesign scientific experimentsDesign subject consent formDetermine potential relationshipsDevelop business planDevelop regulatory strategyDevelop study timelinesdrafting grant applicationsEstablish relationships with Key Opinion LeadersEstablish professional relationships with partnersEthics committee applicationEvaluate licensing opportunitiesFollow up projectsGenerate regulatory submissions Identify market opportunitiesInformed consent processInterpret scientific dataLead studiesLead teamsLiaise with research teamLiaise with doctorsManage budgetsManage regulatory activitiesManage research projectsManage study budgetmanaging a small teamManuscript preparationManufacture of non-GMP batchesManuscript reviewObtain grantsOral presentationOrganise meetingsPrepare final reportPrepare regulatory documentsPresent clinical resultsPresent data at congressproject managementR&DQuality testing of Investigational Medicinal Products (IMPs)Regulatory documentationRegulatory submissionsSupervise analysts and researchers


  • Ph.D. in Biology from KULeuven in 2010
  • Master in Biology from KULeuven in 2006


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency

Area / Region

Lummen, Belgium


Driving License
  • Yes