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Current Experience

  • team leader publication managers

    Since July 2014

  • Publications Manager

    Since October 2010
    coordination of the publication process of Clinical study results in international peer-reviewed journals Coordination of the publication process of clinical study results in international peer-reviewed journals

Past Experience

  • guest professor

    January 2010 --- September 2010

  • BOF postdoctoral scholarship

    January 2007 --- December 2009

  • Clinical Data Manager (DM)

    November 2006 --- January 2007
    company: european organisation of research and Treatment of Cancer, brussels description: Verification and Validation of Clinical research data in Clinical research database.

  • Drug Safety Officer

    August 2006 --- September 2006
    company: bayer, brussels description: assessing and reporting adverse drug reactions to bayer headquarters, germany and belgian Health authorities.

  • PhD student

    October 2001 --- May 2006


Self Assessment :
Analytical thinkingOrganizationWillingness to compromiseAttention to detailApproachabilityCollaborationCreative thinkingCritical thinkingEfficiencyFlexibilityIndependenceInterest in knowledgeProactivityProblem solvingSelf-disciplineService orientedTrustCoordination


Self Assessment :
Understand levels of research evidenceMicrosoft ExcelMedical affairsKnowledge of the drug development processInterpret systematic reviewsInterpret clinical trial resultsInterpret clinical trial resultsImmunologyICH-GCPICH GCP guidelinesGood Clinical Practice (GCP)Efficacy trialsDrug safety assessmentPharmacovigilancePhase ISerious Adverse Event (SAE)Search literature on clinical trialsScientific methodologyRandomization and blindingProtocolProblem-solving methods and troubleshootingPre-clinical researchPowerPointPhases of clinical development (phase I to IV)Phase IVPhase IIIPhase IIDrug Safety and PharmacovigilanceDrug development process NegotiationAntibodiesClinical researchClinical trialsEnglishGCPInfectious diseasesMedical writingMicrosoft OfficeNegotiationPharmaceutical IndustryPrinciples and ethics of clinical research Phase IScientific WritingData ManagementClinical study reportsClinical Study DesignClinical DevelopmentClinical Data Management (CDM)BiopharmaceuticalsBiological Drug DevelopmentAllergy and immunology Scientific writing BiostatisticsProject ManagementTeam LeadershipVaccinesGood Publication Practice (GPP)

Skills and Expertise

Self Assessment :
Validate dataManuscript preparationInteract with pre-clinical scientistsInteract with physiciansExecute scientific projectsDirect co-workersData verificationData validationConduct literature searchesCollaborate with project teamCollaborate with principal investigatorObserve trends in dataOral presentationOrganize scientific projects (in biology)Verify dataSolve problemsReview medical reportsResolves queriesReport study conclusionsReport serious adverse events (SAE)Report dataPresent data at congressPresent clinical resultsPresent at steering committeeCollaborate with medical teamAttend investigator meetingAdverse event reportingmanaging a small teamManuscript preparation and reviewWrite papersSearch literature on clinical trialsReview data interpretationReview clinical study reportsRead medical literaturePublication of articlesNegotiationManuscript reviewOrganise meetingsPublish scientific projectsCommunicate with investigator Search literature on clinical trials Report data Interpret data Analyze dataWritten presentationInterpret dataGuide staffCoach staff Write papers Interact with physicianscoordinate


  • PhD in Biology (zoology) from Ghent University in 2006
  • PhD in Science, Biology from Ghent University in 2005
  • Master in Biology-Zoology from Universiteit Gent in 2001


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
  • International:


    Expert has 14 publications (Will be avalible with full profile)

Area / Region



Driving License
  • Yes

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