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a medical Scientist with a broad knowledge of Medicine, Neuroscience and experience in functional neuro-imaging studies on human subjects. i thoroughly enjoy working in an international and multidisciplinary environment and am driven by an avid interest in Healthcare, Data Science and Innovation.


Current Experience

  • PhD student

    Since October 2012
    targid TARGID

Past Experience

  • Medical student

    January 2008 --- July 2012

  • Intern (Medical Doctor) Shanghai, China

    January 2008 --- January 2009


Self Assessment :
CommunicativeResponsibilityCollaborationOrganizationAttention to detailAdaptabilityEfficiencyCuriosityInterest in knowledgeCreative thinkingFlexibilityIndependenceService orientedProactivity


Self Assessment :
MedicineNutritionClinical Study DesignTeamwork Negotiation R&DAnalysis Biostatistics Phase IPhase IIR Scientific writingEthics submission and approval processClinical Data Management (CDM)Clinical researchClinical study reportsData ManagementData AnalysisData cleaningGood Clinical Practice (GCP)Human AnatomyInternal medicineMatlabMedical writingMicrosoft ExcelMicrosoft OfficeMedical ImagingMicrosoft PowerpointMicrosoft WordNegotiationPhysiologyPresentation SkillsProblem SolvingPrinciples and ethics of clinical researchProgrammingProtocolPsychiatryQuality Control (QC)Randomization and blindingRecruitingReport WritingResearchAdverse Events (AE)Data entrySASscienceScientific CommunicationsScientific WritingSocial SkillsSocial MediaStatisticsGastroenterologyEnglishOutlookInformed Consent DocumentsUnderstand how results translate to practiceBiomedical SciencesElectrocardiogram (ECG)Health EconomicsIt skillsStatistical Data AnalysisPreclinical Research
LinkedIn Assessment :
ResearchscienceData AnalysisLife SciencesStatisticsClinical researchHospitalsHealthcareMedicinePublic SpeakingNeuroscienceSPMSASMicrosoft OfficeRfMRI

Skills and Expertise

Self Assessment :
Analyze data Control data Develop clinical trial protocols Guide students Interact with nurses Interact with physicians Monitor a clinical study Report data Search literature on clinical trials Write papersAdjust processes and methodsAdvise on medical perspectivesWriting regulatory documentsWrite medical reportswrite and maintain clinical evaluation reportsWork with coordination and data management teamsSupervise data processingSolve problemsSet up a clinical studyArchive documentationAssess subject safetyAssure medical qualityCalculate timelines for conducting and completing the trialCapture data on source documentsCollaborate with project teamCommunicationConduct literature searchesConduct research at universitiesConduct studiesConduct the trialConduct university research Confirm protocol complianceCoordinate ethics committeeCoordinationCreate clinical documentsCreate clinical project documents according to the protocolDesign clinical trialDetermine availability of facilities and equipment at the siteDetermine needsDetermine potential relationshipsDevelop clinical hypothesesDiscuss treatments with investigatorEnsure consistency between the protocol and CRFEnsure data consistencyEnsure good clinical practice (GCP)Evaluate protocolsGastrointestinal diseasesIdentify risksInteract with physiciansInteract with pre-clinical scientistsInteract with pharmacistsInteract with statisticiansInterpret dataLiaise with doctors and other professionals throughout the studyLiaise with research team in order to accurately collect and record dataManage risksManage research projectsReview dataPresent data at congressPlanning clinical studiesParticipate in medical reviewOral presentationNetworkNegotiationMonitoring enrolmentManage clinical trial files/documentsQuality control processRSasmatlabAdministrative supportResearch at universitiesWrite statistical reportscollaborate in research projects at universities


  • Ph.D. student in Medicine from KU Leuven in 2017
  • master in clinical medicine from Shanghai Jiao Tong University in 2012

Training and Certification

  • Doctorate in 2017 Training
  • Medical Doctor in 2012 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Full Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Associate Scientist Biomedical Scientist BioStatistician Clinical Trial Assistant (CTA) Data Scientist Post-doctoral Fellow Research fellow
  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:


    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Leuven, Belgium


Driving License
  • No

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