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Current Experience

  • Senior Clinical Research Associate (CRA)

    Since October 2016

Past Experience

  • Senior Clinical Research Associate (CRA) Vilvoorde, Belgium

    September 2010 --- October 2016


Self Assessment :
Analytical thinkingAttention to detailCollaborationEfficiencyOrganization


LinkedIn Assessment :
Fluent EnglishAble To Multi-taskTime ManagementDeadline OrientedOversightPeople SkillsFlexible SchedulingCROCTMSEnglishICH-GCPLife Sciences

Skills and Expertise

Self Assessment :
Coach and provide guidance to clinical staff. Analytical skills Assure medical quality Interact with nurses Interact with physicians Interpret data Monitor a clinical studyAct as the main line of communication between the sponsor and the investigatorAdjust processes and methodsAdminister, maintain and co-ordinate the logistical aspects of clinical trialsAnswer, transfer and handle incoming calls as needed.Approve monitoring reportsApprove queriesAssess adverse reactionsAssess site feasibilityAssess subject safetyAssist study siteAssist with site trainingAssist with proceduresAttend investigator meetingClinical data collectionCollaborate with medical teamCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Communicate with investigatorCommunicate with sponsorConduct close-out visitsConduct maintenance visitsConduct site initiationConduct supply issue resolution activitiesConfirm protocol complianceData validationData verificationDetermine availability of facilities and equipment at the siteDevelop ICH/GCP compliant processesDevelop training materialsDirect co-workersDiscuss treatments with investigatorDistribute study documentsEnsure consistency between the protocol and CRFEnsure good clinical practice (GCP)Estimate subject complianceFacilitate sponsor monitoring visitsFollow-up of external auditsGastrointestinal diseasesIdentify and provide training to trial team and associated staffInteract with pharmacistsManage clinical suppliesManage clinical trial files/documentsManage Clinical Trial Management System (CTMS) Manage multiple projectsMonitor dataMonitoring enrolmentMonitoring subject complianceObserve trends in dataOral presentationPrepare external auditsRetrieve study documentsReview exclusion criteriaReview inclusion criteriaReview informed consent processReview medical reportsReview monitoring reportsReview queriesSchedule trial visitsSerious Adverse Event (SAE) ReconciliationSite managementSolve problemsTeachingUnderstand protocolsUpdate Clinical Trials Management System (CTMS) Work collaboratively with the other members of the clinical research team Work cross-functionallyWork under specific instructions


  • Master in Biomedical Sciences in Neuroscience from University of Antwerp in 2010
  • Latin-Maths in from Koninklijk Atheneum Boom in 2005

Training and Certification

  • ICH GCP Barnett in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Full Proficiency

Area / Region



Driving License
  • Yes

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