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Current Experience

  • Research assistant

    Since May 2013

Past Experience

  • Clinical Research Associate (CRA)

    September 2012 --- March 2013
    function description: *on-site monitoring of Clinical trials in belgium and luxembourg (verify science)" rel="nofollow">Protocol Compliance & regulatory/ich gcp Compliance, monitoring of Adverse Events, ...) *in-house monitoring activities indications: *glaucoma *non-small Cell lung Cancer key competences: *build relationships with investigators and site staff *Problem-solving skills *excellent interpersonal, verbal and written Communication Skills *knowledgeable about local regulations in belgium and luxembourg *knowledgeable about ich-gcp


Self Assessment :
CollaborationCritical thinking


Self Assessment :
Cell biologyClinical monitoringClinical trialsEnglishEthics submission and approval processGeneticsGood Clinical Practice (GCP)Informed Consent ProcessInterpret systematic reviewsPhases of clinical development (phase I to IV)Principles and ethics of clinical researchQuality of Life (QoL) outcomesSchizophreniaSearch literature on clinical trialsUnderstand levels of research evidenceInformed Consent Documents Animal modelsActions and modes of action of drugs in the human speciesCancerClinical Study DesignMedical oncology OphthalmologyPediatrics
LinkedIn Assessment :
Clinical trialsICH-GCPClinical monitoringResearch EthicsMedical EthicsClinical research

Skills and Expertise

Self Assessment :
Interact with ethics committeeInteract with physiciansProvide trainingResolves queriesSchedule sponsor monitoring visitsTrain on site staffVerify data Interact with nurses Interact with physicians Monitor a clinical study Search literature on clinical trials Write papersAdverse event reportingAssist study siteCommunicate with investigatorCommunicate with sponsorConduct monitor visitsConduct research at universitiesConduct site initiationData validationData verificationEnsure data integrityEnsure good clinical practice (GCP)Estimate subject complianceInteract with CROs


  • Postgraduate Master in Bio-Ethics from Katholieke Universiteit Leuven, Radboud Universiteit Nijmegen, Università degli studi di Padova in 2012
  • Master of Science (M.Sc.) in Biomedical Sciences from Katholieke Universiteit Leuven in 2011
  • Bachelor of Science (B.Sc.) in Biomedical sciences from Katholieke Universiteit Leuven in 2009

Training and Certification

  • FELASA B- certificate in 0000 Certification
  • Personal First Aid / CPR in 0000 Certification
  • Youth Animator Certificate in 0000 Certification

Work Preferences

  • Notice Period:
    10 weeks
  • Work From Home:
    Yes, 0 to 2 days per week
  • International:

Area / Region

Leuven, België


Driving License
  • Yes

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