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Current Experience

  • Clinical Readouts Team leader for MMR/V and Zoster

    Since March 2014
    Assay development I am the central point of contact for different bodies within GSK as well as with external collaborators/stakeholders when discussions are related to Clinical Readouts, vaccine immunogenicity and correlates of protection. I ensure the scientific and clinical relevance of the clinical immunology testing to document the immunogenicity of the vaccine and identify correlates of protection. I develop testing strategies taking into account of the scientific relevance, the technical feasibility and regulatory requirements. I lead the Clinical Readout Team, composed of assay development experts, clinical development managers and regulatory authority experts to ensure alignement within the project and achieve project milestones.

Past Experience


Self Assessment :
Analytical thinkingCollaborationCommunicativeCoordinationIndependenceOrganizationResult OrientedSelf-disciplineTrust


Self Assessment :
Biochemistry R&DAnalytical techniquesBiological Drug DevelopmentClinical DevelopmentClinical researchClinical study reportsClinical trial designClinical trialsCross-functional team leadershipeCTDEnglishCMCImmunoassaysPhases of clinical development (phase I to IV)Project ManagementRegulatory affairsRegulatory submissionsTeamworkVaccines
LinkedIn Assessment :
Regulatory affairsClinical DevelopmentMatrix ManagementClinical researchRegulatory submissionsPharmaceutical IndustryVaccinesInfluenzaClinical Study DesignClinical trialsProtocol ReviewICH-GCPImmunologieExigences rBiotechnologieBonnes pratiques cliniquesDSOPMaladies infectieuses

Skills and Expertise

Self Assessment :
Collaborate with project teamCommunicationcoordinating research projectsCoordinationInteract with pre-clinical scientistsInteract with regulatory stakeholdersInteract with statisticiansLiaise with research teamManage multiple projectsManage regulatory activitiesManage research projectsPrepare regulatory documentsproject managementProvide input to process improvement initiativesProvide support for scientific and/or technical projectsR&DRegulatory submissionsReview clinical study reportsReview dataReview study protocolsReview the interpretation of dataSolve problemsWork collaboratively with the other members of the clinical research team Work cross-functionallyWrite documentsWriting regulatory documents


  • PhD in Biochemistry and Biophysics from Faculté universitaire des Sciences agronomiques de Gembloux in 2007
  • M2R in Biology, Health, Biotechnology from Université Paul Sabatier (Toulouse III) in 2003


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


    Expert has 3 publications (Will be avalible with full profile)

Area / Region

Ramillies, Belgium


Driving License
  • Yes

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