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- coordinate the functionaliteit team members and their activities - communicate with sponsors, internaliseer departments, vendors and internal team members - confirm adherence to study requirements and tuimelingen - prepare and review study guidelines and materials User by the Clinical team - review and approve visit reports - plan and manage resource issues - identify and follow up quality issues until resolution - provider guidance and support to all study team members - oversee maintenance and quality checks of study files


Current Experience

  • Clinical Trial Manager (CTM) Leuven, Belgium
    Since February 2016

Past Experience

  • Sr Clinical Operations Leader
    November 2015 --- January 2016

  • Clinical Operations Leader
    November 2012 --- October 2015

  • Associate Clinical Operations Leader
    June 2010 --- November 2012

  • Senior Clinical Research Associate
    October 2008 --- May 2010

  • Senior CRA - Team Leader
    September 2007 --- September 2008

  • Clinical Research Associate (CRA)
    October 2002 --- August 2007

  • Clinical Research Associate (CRA)
    March 2002 --- August 2002


Self Assessment :
Attention to detailWillingness to compromiseProblem solvingProactivityKindnessInterest in knowledgeFlexibilityEfficiencyCreative thinkingCritical thinkingCollaborationSelf-discipline


Self Assessment :
Diabetes Medical devicesAllergy and immunologyBiological Drug DevelopmentCancerCardiologyCardiovascular diseasesClinical DevelopmentClinical Data Management (CDM)Clinical operationsClinical monitoringClinical researchClinical trial managementClinical trialsCross-functional team leadershipDermatologyTeam LeadershipInformed Consent ProcessVascular surgeryStem cell researchSports medicineSupervising CRAsSOPSerious Adverse Event (SAE)RheumatologyData cleaningElectronic Data Capture (EDC) EndocrinologyEnglishGood Clinical Practice (GCP)Gynecologic oncologyICH GCP guidelinesMicrosoft ExcelMicrosoft OfficeNephrologyPatient Screening and RecruitmentPhase IIIPhase IIPhase IVPhysical medicine and rehabilitationPowerPointPrinciples and ethics of clinical researchProject ManagementQualification
LinkedIn Assessment :
Clinical researchClinical monitoringClinical trialsCROClinical Research AssociatesClinical operationsICH-GCPGCPElectronic Data Capture (EDC) Clinical DevelopmentTherapeutic AreasCTMS

Skills and Expertise

Self Assessment :
Interact with physicians Monitor a clinical studyAdjust processes and methodsAdverse event reportingApprove monitoring reportsArchive study documentsAssess site feasibilityAssess subject safetyAttend investigator meetingBuild trial master file (TMF)CoachCollaborate with medical teamCollaborate with principal investigatorCollaborate with project teamCommunicate with investigatorCommunicate with sponsorComplete case report form (CRF)Conduct site initiationConduct the trialConfirm protocol complianceCoordinate ethics committeeCreate clinical documentsCreate study documentsCreates a collaborative team environmentData verificationDetermine potential relationshipsDocument adverse eventsDocument employees training requirementsEnsure good clinical practice (GCP)Estimate subject complianceFollow-up of external auditsFollow-up of internal auditsIdentify investigatorsInitiation visitInteract with nursesInteract with pharmacistsInteract with physiciansManage clinical trial files/documentsManage Clinical Trial Management System (CTMS) Manage contractors Manage projects resourcesManage study supplyManage subject consent formManage trial master file (TMF)Monitor a clinical studyMonitor clinical trials Oral presentationPatient recruitmentProtocol managementProvide benefit risk assessmentProvide trainingRespond to audit findingsReview exclusion criteriaReview inclusion criteriaSchedule trial visitsSelect investigatorsSerious Adverse Event (SAE) ReconciliationSite managementStudy-related documentsSupervise clinical monitorsTrain off site staffTrain on site staff


  • MSc in Physiotherapy from Katholieke Universiteit Leuven in 1996

Training and Certification

  • Sports physical therapist in 2000 Certification


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

Work Preferences

  • Notice Period:
    12 weeks
  • Work From Home:
    Yes, 1 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region



Driving License
  • Yes