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Experiences

Current Experience

  • Clinical Research Associate (CRA) Homebased Leuven
    Since September 2015

    Working closely with Field CRA's, Clinical trial managers, SSU,... to monitor hospital sites on compliance to GCP, this off-site as well as on-site. My responsibilities include: FDA submissions, Filing, query resolution and helping out the site with the daily problems in clinical research e.g. ordering kits, tracking deliveries, looking up compliances with protocol ect.

Past Experience

  • Clinical Trial Assistant (CTA) Leuven, Belgium
    March 2015 --- August 2015

    Responsible for executing the study protocols according to GCP. This entails coordination of patient visits, scheduling of all procedures requested by protocol, communication with patients, collecting and reporting of data into the eCRF, reporting of SAEs to the sponsor.

Personality

Self Assessment :
SociabilityAnalytical thinkingOrganizationAdaptabilityAssertivenessCommunicativeCreative thinkingFlexibilityKindnessInterest in knowledgeProblem solvingResponsibilityStrategic thinking

Knowledge

Self Assessment :
Biochemistry Cell biology Labtechnician Phase I R&D Scientific writingAnalysisAllergy and immunologyAnalytical methodsAnalytical proceduresAnalytical techniquesAseptic TechniquesBiochemistryBiomedical EngineeringBiotechnologieCancer ResearchCancerCardiovascular diseasesChromatographyClinical monitoringClinical DevelopmentClinical trialsClinical researchCROELISAEnglishGood Clinical Practice (GCP)HematologyICH guidelinesIn VitroIn VivoLaboratory ResearchMicrobiologyOutlookPhase IIPhase IIIProtein PurificationqPCRRadiologyRNA isolationRT-PCRTeamworkGCLiquid chromatography–mass spectrometry (LC-MS)Documentation

Skills and Expertise

Self Assessment :
Interact with physicians Molecular DiagnosticsAseptic techniquesCell cultureData entryEnsure good clinical practice (GCP)lifesciencepcrR&DSolve problemsUnderstand protocolsUse laboratory techniquesUse western blotting techniqueSchedule trial visits Analytical skills Analyze data Monitor a clinical study Use a confocal microscopyAssist with experimentsAttend investigator meetingAttend seminarsInterpret research resultsInterpret analytical results

Education

  • Master in Biochemical Engineering from GroepT KULeuven in 2015
  • Bachelor in Biomedical Laboratory Techniques from Katholieke Hogeschool Leuven in 2012

Training and Certification

  • CPR in 2015 Certification
  • Good clinical practice in 2015 Certification
  • JCI Presenter in 2015 Certification
  • Lab Animal Handling in 2015 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Professional Proficiency
French
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Biomedical Scientist Chemical Analyst Clinical Laboratory Technician Doctoral Researcher Junior Scientist Lab Analyst Lab Scientist Lab Technician (Toxicology) Laboratory Engineer Laboratory Technologist Molecular Biologist Ph.D. Student PhD researcher Project Engineer QA Engineer Research Scientist Scientific Researcher Scientist
  • Locations I am interested in:
    Antwerp, Belgium Brussels, Belgium Leuven, Belgium Mechelen, Belgium
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Leuven, Belgium

Others

Driving License
  • Yes