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Past Experience

  • Master Thesis Leuven, Belgium

    September 2014 --- September 2015

    work with clinicians in uz leuven to study the ivf patients’ profiles. aim to find prognostic factors that affects ivf success rate:

    • communicate with clinicians to acquire and pre-process data;

    • conduct Data cleaning, including coding medical events, checking database for inconsistency and missing, generating queries;

    • propose and decide analytic techniques according to the Research aim;

    • conduct Statistical analysis (mixed model, longitudinal Data Analysis, missing data imputation, random forest algorithm), interpret results and report on regular basis.

  • Research associate Singapore

    August 2011 --- August 2013

    involved in a collaboration with the Pharmaceutical company gsk shanghai,

    and lead a pre-Clinical compound Testing project:

    • design and conduct Laboratory experiments for Testing an novel drug;

    • collect experimental data and perform Statistical Analysis (two-way anova, multiple comparison);

    • communicate with the collaborating Pharmaceutical company, update results and finalize report in due time.


Self Assessment :
AdaptabilityAnalytical thinkingAttention to detailCollaborationCritical thinkingEfficiencyFlexibilityIndependenceInnovative thinkingKindnessOptimismOrientationProblem solvingReaction to stressResult Oriented


Self Assessment :
BiostatisticsStatistical Data AnalysisStatisticsClinical researchDesigning case report formsDrug regulatory authoritiesFluorescence MicroscopyGel ElectrophoresisImmunofluorescenceInterpret clinical trial resultsLaboratory ResearchMammalian Cell CultureOxidative stressPre-clinical researchrecombinant DNA technologyReport WritingResearchStem cell researchWriting Study Procedures and SOPsUnderstand levels of research evidenceAnalytical proceduresCell CultureElectrophoresisInterpret clinical trial resultsPresentations

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Design case record forms Interpret data Report data Search literature on clinical trials Use a confocal microscopy Write papersConduct animal studiesConfocal microscopyCreate standard operating procedure (SOP)Data analysisInterpret dataInterpret analytical results


  • Master in Statistics in Clinical Trials and medicine from KU Leuven in 2015
  • Ph.D. in Biomedical Sciences from National University of Singapore in 2013


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Trial Assistant (CTA) Biomedical Scientist Lab Scientist statistician Data Analyst Clinical Data Manager (DM) Clinical Data Reviewer Data Reviewer Data Manager Medical Data Coordinator
  • Locations I am interested in:
  • Work From Home:
  • International:

Area / Region

Aalst, Belgium


Driving License
  • Yes

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