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Current Experience

  • Clinical Research Associate (CRA)

    Mechelen, Belgium
    Since May 2015

Past Experience

  • Clinical Data Manager (DM) Mechelen, Belgium

    September 2012 --- April 2015


Self Assessment :
AdaptabilityApproachabilityAttention to detailCollaborationCommunicativeCompetitivenessCoordinationCuriosityDependabilityEfficiencyFlexibilityInnovative thinkingInterest in knowledgeKindnessOptimismOrganizationProblem solvingResponsibilityResult OrientedSociability


Self Assessment :
Animal models Phase I Medical devices21 CFR Part 11Adverse Events (AE)Biological Drug DevelopmentBiomedical SciencesCDISCClinical Data ManagementClinical Data Management (CDM)Clinical monitoringClinical operationsClinical researchClinical Study DesignClinical study reportsClinical trial budgetingClinical trial designClinical trial managementClinical Trial Management System (CTMS)Clinical trialsCommunication SkillsComplianceCRFCRF designCROCurrent Good Manufacturing Practice (CGMP)Data AnalysisData cleaningData entryData ManagementDatabase design and maintenanceDatabasesDrug DeliveryDrug Safety and PharmacovigilanceDrug safety assessmentEarly development stageeCRFEDCElectronic Data Capture (EDC) ELISAEnglishEnzyme-linked immunosorbent assay (ELISA)Ethics submission and approval processFDAGeneticsGMPGood Clinical Practice (GCP)Good Clinical Practice Veterinary (GCPv)Good Laboratory Practice (GLP)Good Manufacturing Practice (GMP)Informed Consent DocumentsInformed Consent ProcessIVRSLife SciencesMicrosoft ExcelMicrosoft OfficeMicrosoft PowerpointMicrosoft WordMonitoring Study ProgressNeuroscienceoncoOncology Clinical ResearchOutlookPatient Follow UpPatient Screening and RecruitmentPCRPharmacodynamicsPharmacokineticsPhase IPhase IIPhase IIIPhase IVPhases of clinical development (phase I to IV)PowerPointPresentationsProject PlanningProject ManagementRespiratorySerious Adverse Event (SAE)Social SkillsSPSSStandard Operating Procedure (SOP)Study approvalsTime ManagementTrainingWriting Study Procedures and SOPs

Skills and Expertise

Self Assessment :
Build and manage the Trial Master File (TMF) Create SOPs Design case record forms Interact with nurses Interact with physicians Monitor a clinical study Report data


  • Master in Biomedical Sciences from University of Antwerp in 2012


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Locations I am interested in:
    2300 Turnhout, Belgium 2321 Hoogstraten, Belgium 2390 Malle, Belgium Beerse 2340 Belgium Geel, Belgium Lille, Belgium Mol, Belgium Zoersel, Belgium
  • Work From Home:
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region

Oud-Turnhout, Belgium


Driving License
  • Yes

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