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executive manager at  aurora medical support belgium (amsb) and Freelancer clinical research

amsb: support to clinical research and medical professionals, including but not restricted to : translations (English, French and German to dutch), trainings, writing of medical articles, Data entry, Data Management, Clinical Research Associate


Current Experience

  • Senior Clinical Research Associate (CRA)

    St Niklaas, Roeselare, Lausanne
    Since January 2018

  • Study Team Leader

    Amsterdam, Antwerp, Beverwijk
    Since October 2016

  • Senior Clinical Research Associate

    France, The Netherlands, Belgium
    Since February 2014


Self Assessment :
AssertivenessSociabilitySelf-confidenceSelf-disciplineProblem solvingProactivityOrganizationOptimismInterest in knowledgeIndependenceFlexibilityEfficiencyCoordinationCollaborationAttention to detailApproachabilityWillingness to compromise


Self Assessment :
Clinical trial audits and inspectionsClinical trialsData cleaningData entryData ManagementDrug Safety and PharmacovigilanceElectronic Data Capture (EDC) EndocrinologyGCPGood Clinical Practice (GCP)HospitalsICH GCP guidelinesInformed Consent ProcessMedical consultingNeurologyoncologyOphthalmologyPatient Follow UpPatient Screening and RecruitmentPharmacovigilancePhases of clinical development (phase I to IV)Serious Adverse Event (SAE)ToxicologyUnderstand how results translate to practiceInformed Consent Documents Diabetes Medical devices Negotiation Scientific writingCancerClinical Data Management (CDM)Clinical DevelopmentClinical monitoringClinical research

Skills and Expertise

Self Assessment :
Control data Guide students Interact with nurses Interact with physicians Monitor a clinical studyAlzheimerAttend seminarsAttend investigator meetingClinical data collectionCoachCollaborate with medical teamCollaborate with principal investigatorCollaborate with project teamCollect patient forms and questionnairesComplete case report form (CRF)Conduct close-out visitsConduct monitor visitsConduct post-marketing surveillance studyCreate study documents Write papersDocument adverse eventsmanaging a small teamManuscript preparation and reviewMonitor clinical trials Oral presentationParticipate in medical reviewPrepare external auditsPrepare internal auditsRead medical literatureResolves queriesTranslate protocol into packaging and labeling requirementsVerify dataWrite medical reportsWrite papers Build and manage the Trial Master File (TMF)


  • Bachelor in Nursing from University Leuven in 1979

Training and Certification

  • Train the Trainer in 2013 Training
  • Monitor Visits in 2011 Training
  • People Management in 2006 Training
  • Time Management in 2006 Training
  • Audit ISO 9001 in 2014 Certification
  • ICH/GCP in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    12353|data entry|1677|coach|6141|551|177
  • Locations I am interested in:
    Belgium France The Netherlands
  • Work From Home:
    Yes, 1 to 5 days per week
  • Work Regime:
    BrightOwl freelancer :    20 Hours per week
  • International:
  • Availability:
    Mar 2018 : 50%
    Apr 2018 : 50%
    May 2018 : 50%
    Jun 2018 : 50%
    Jul 2018 : 50%

Area / Region

Antwerpen, België


Driving License
  • Yes

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