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Summary

 involved in monitoring activities and the site management of Clinical trials with following Medical Devices:

 

-bifurcation stent in coronary artery lesions (the netherlands, uk, france, ireland)

-drug eluting balloon systems in peripheral artery lesions (germany, belgium)

-first in man evaluation of a large hole (18 to 24f) percutaneous Vascular closure device (belgium, ireland, germany)

-flow diverting device for the Treatment of intracranial aneurysms (germany, france,uk, italy)

-cryo ablation catheter for the Treatment of atrial flutter (belgium, the netherlands)

Experiences

Past Experience

  • Clinical Research Associate (CRA)

    September 2013 --- November 2014

  • Intern

    November 2012 --- June 2013
    master thesis

  • Intern

    May 2012 --- June 2012

  • Summerschool in Radiobiology

    August 2011 --- August 2011

Personality

Self Assessment :
Attention to detailCritical thinkingFlexibilityIndependence

Knowledge

Self Assessment :
Cardiovascular diseasesClinical monitoringClinical researchClinical trialsClinical trial managementGood Clinical Practice (GCP)ICH-GCPMedical ImagingMicroscopyMicrosoft ExcelMicrosoft OfficePowerPoint Medical devicesBiotechnologyCardiology
LinkedIn Assessment :
Biomedical SciencesMolecular ImagingMRIPositron Emission TomographyDiffusion Tensor ImagingEnglishFrenchdutchMedical DevicesClinical trialsGCP

Skills and Expertise

Self Assessment :
Control data Interact with nurses Interact with physicians Monitor a clinical study Use a confocal microscopyAdverse event reportingCapture data on source documentsConduct monitor visitsComplete case report form (CRF)Collaborate with medical teamCollaborate with principal investigatorCommunicate with investigatorCommunicate with sponsorConduct site initiationCoordinate with the ethics commiteeData verificationInitiation visitInformed consent processInteract with ethics committeeInteract with nursesInteract with physiciansLiaise with research teamVerify dataTrain on site staffStudy-related documentsSite managementReview data interpretationReport serious adverse events (SAE)Report deaths to regulatory authoritiesRead medical literatureProvide study site fileMonitoring enrolmentMonitoring subject complianceMonitor dataMonitor clinical trials

Education

  • Master in Specifieke Lerarenopleiding from Universiteit Antwerpen in 2015
  • Master of Science (MS) in Molecular imaging from Universiteit Antwerpen in 2012
  • Bachelor's degree in Biomedical Sciences, General from Universiteit Antwerpen in 2011
  • Europees baccalaureaat in Wetenschappen - wiskunde from Europese School Mol in 2008

Training and Certification

  • Felasa type C in 0000 Certification

Languages

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

Work Preferences

  • Notice Period:
    1 week
  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    Permanent position
    BrightOwl freelancer
  • International:
    No

Area / Region

Antwerpen, België

Others

Driving License
  • Yes

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