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Current Experience

  • Clinical Research Associate (CRA)

    Lasne, Belgium
    Since January 2017

    as a Clinical Research Associate, you are the primary contact for Hospitals participating in Clinical trials. list of the responsibilities (not exhaustif):

    • comprehension of science)" rel="nofollow">Protocol and monitoring guidelines
    • participate in Investigator meetings
    • site selection visits
    • contract negociations
    • faisability questionnaires
    • site initiation visits
    • monitoringvisits + study follow-up by phone/e-mail
    • close out visits
    • reporting

    currently i have 1 Phase II study in stemcells; 2 phase 4 studies in Nephrology and oncology

    As a Clinical Research Associate, you are the primary contact for hospitals participating in clinical trials. List of the responsibilities (not exhaustif):

    • Comprehension of Protocol and monitoring guidelines
    • Participate in investigator meetings
    • Site selection visits
    • Contract negociations
    • Faisability questionnaires
    • Site initiation visits
    • Monitoringvisits + study follow-up by phone/e-mail
    • Close out visits
    • Reporting

    Currently I have 1 phase II study in Stemcells; 2 phase 4 studies in nephrology and oncology

Past Experience

  • Clinical Support Specialist

    October 2012 --- October 2016

    1/ Sales support

    • assume primary responsibility Sales support in europe and provide Sales support in all other markets as required
    • identify new Sales opportunities in europe & row areas
    • provide Sales support at industry meetings as required.
    • provide product demonstration sessions for new Sales leads

    2/ Clinical affairs

    • develop and keep up to date Sales tools and Presentations and collaborate with Marketing and Communication to have them approved
    • identify opportunities and assist customers with data collection and Analysis to facilitate creation of manuscripts and writing papers involving our products and services.
    • identify latest scientific abstracts and Publications and insure that ors staff receives recent updates on a regular bases
    • attend scientific sessions during industry meetings and identify latest needs and developments
    • contribute to new product launches
    • assist in setting up regional; national and international symposia
    • coordinate the submission of tenders

    3/ product implementations and customer Training

    • provide perfusion Consulting services
    • provide lifeport Training to new and existing customers
    • install and support product upgrades
    • provide Clinical customer support


    September 2011 --- August 2012
    master thesis

  • Graduate student

    September 2007 --- July 2012

    master Biomedical Sciences


Self Assessment :
AdaptabilityAnalytical thinkingCollaborationCommunicativeCompetitivenessCritical thinkingCuriosityEfficiencyFlexibilityResult OrientedStrategic thinkingTrustApproachabilityAuthenticityCreative thinkingIndependenceInnovative thinkingInterest in knowledgeKindnessOptimismProactivityProblem solvingReaction to stressWillingness to compromise


Self Assessment :
Biochemistry Negotiation Scientific writingBiomedical SciencesBusiness DevelopmentClinical Data ManagementClinical researchCommunication SkillsCustomer ServiceData AnalysisData cleaningEnglishGastroenterologyHealthcareKOL managementLife SciencesMarket researchMarketing CommunicationsMedical Device R&DMedical DevicesMedical ImagingMicrosoft OfficeMicrosoft PowerpointMicrosoft ProjectMicrosoft WordMicrosoft ExcelMultilingualNephrologyNutritionOutlookOutsourcingPowerPointProduct managementSalesTrainingTroubleshootingAdverse Events (AE)Aseptic TechniquesCancer ResearchCAPACE CertificationClinical monitoringClinical operationsClinical Study DesignClinical study reportsCompliance with regulationsCRFCROCTMSeCRFEDCElectronic Data Capture (EDC) Good Clinical Practice (GCP)Hospital SalesInformed Consent DocumentsInformed Consent ProcessInternational RelationsLifesciencesMarket AnalysisMarket developmentMarketingMarketing StrategyMedical affairsNegotiationOncologOncology Clinical ResearchPharmaceutical ResearchPhase IIPhase IIIPhase IVPhases of clinical development (phase I to IV)Standard Operating Procedure (SOP)Teamwork
LinkedIn Assessment :
scienceScientific WritingLifesciencesPCRmolecular biologyNeuroscienceClinical researchClinical trialsCell biologyHealthcareMicroscopyPharmaceutical IndustryBiotechnologyLife SciencesMedical Devices

Skills and Expertise

Self Assessment :
Interact with physicians Interact with nurses Interpret data Lab scale batches Report data Search literature on clinical trialsAseptic techniquesAssemble regulatory applicationsAssist with experimentsAssist study siteAssist with site trainingAssure medical qualityAttend seminarsCollaborate with medical teamCollaborate with principal investigatorCommunicationConduct literature searchesCreate SOPsDevelop training materialsFollow up training programsInteract with KOLInteract with nursesInteract with physiciansInterpret dataInterpret scientific dataLiaise with doctorsLiaise with doctors and other professionals throughout the studyMaintenance of biomedical equipmentOral presentationProvide trainingProvide technical supportRead medical literatureTrain off site staff


  • Master's degree in Biomedical Sciences, General from University of Leuven in 2012
  • Master of Science; Bachelor of Arts in Biomedical Sciences; Laboratory Animal Science from Universidad de Salamanca in 2010
  • Bachelor of Arts (B.A.) in Linguistics from University of Leuven in 2007


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

Work Preferences

  • Work From Home:
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region



Driving License
  • Yes


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