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Self Assessment :
ApproachabilitySociabilityTrustSelf-disciplineKindnessInterest in knowledgeIndependenceDependabilityCritical thinkingCollaborationOrganization


Self Assessment :
R&D Scientific writingEnglishGermanGood Laboratory Practice (GLP)HPLCInterpret systematic reviewsMedical writingMicrosoft OfficeOxidative stressScientific methodologyScientific WritingSearch literature on clinical trialsWriting Study Procedures and SOPsAnalytical methodsAnalytical techniquesChromatographyClinical monitoringClinical researchClinical trialsEthics submission and approval processGood Clinical Practice (GCP)Good Publication Practice (GPP)Grant WritingGrant PreparationICH guidelinesInformed Consent DocumentsInformed Consent ProcessISO 17025Laboratory ResearchLife SciencesLiquid Chromatography-UV (LC-UV)Microsoft PowerpointMicrosoft WordMicrosoft ExcelNMRNutritionOutlookPharmaceutical ResearchPreclinical ResearchPurificationQuality Assurance (QA)Report WritingResearchScientific CommunicationsSerious Adverse Event (SAE)SpectroscopyTeamworkUnderstand levels of research evidenceValidation

Skills and Expertise

Self Assessment :
Analyze data Create SOPs Guide students Report data Search literature on clinical trials Write papersWritten presentationWrite protocolsWrite combined statistical and medical reportsVerify dataValidate dataSolve problems Develop protocolsAttend seminarsCollaborate with project teamConduct research at universitiesConduct university research drafting grant applicationsExtrapolate dataInteract with pharmacistsInterpret data Assure medical qualityOrganize scientific projects (in biology)Publication of articlesPublish scientific projectsResearch at universitiesReview study protocolsRespond to audit findingsRead medical literatureManuscript preparation and review Analytical skills Control data Interpret data Monitor a clinical study Write protocolsAdverse event reportingApprove consent documentsAttend seminars, courses and meetings within and outside the companyClinical data collectioncollaborate in research projects at universitiesCommunicationConduct literature searchescoordinating research projectsCreate SOPsDevelop ICH/GCP compliant processesDevelop protocolsEnsure good clinical practice (GCP)Ethics committee submissionsExecute scientific projectsGuide studentsInformed consent processInteract with ethics committeeInterpret scientific dataInterpret research resultsManage research projectsManuscript preparationMonitor dataObtain grantsPlan experimentsPrepare manuscriptR&DRead medical literature to maintain current awareness and knowledgeReport serious adverse events (SAE)Review the interpretation of dataSet up research projectsStudy-related documentsSupervise PhD studentsSupervise techniciansTeachingSupervise trial suppliesUnderstand protocolsWrite documentsWrite papers


  • Ph.D. in Pharmaceutical Sciences from University of Antwerp in 1995

Training and Certification

  • CRA Responsibilities in 2016 Training
  • ICH-GCP G6 Guideline in 2016 Training
  • BELTEST course Technical Auditor EN45001 in 1999 Training
  • Introduction to ICH-GCP Guidelines (Association of Clinical Research Professional) in 2016 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency
Professional Proficiency
Professional Proficiency

Work Preferences

  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:

Area / Region



Driving License
  • Yes