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 science)" rel="nofollow">Protocol ect.
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.
Clinical Trial Assistant (CTA) Leuven, BelgiumMarch 2015 --- August 2015
responsible for executing the study protocols according to gcp. this entails coordination of patient visits, scheduling of all procedures requested by science)" rel="nofollow">Protocol, Communication with patients, collecting and reporting of data into the eCRF, reporting of saes to the sponsor.
SociabilityAnalytical thinkingOrganizationAdaptabilityAssertivenessCommunicativeCreative thinkingFlexibilityKindnessInterest in knowledgeProblem solvingResponsibilityStrategic thinking
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 chromatographyDocumentation
Skills and Expertise
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
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