BrightOwl Loader Loading


Current Experience

  • Medical information /affairs manager Brussels
    Since September 2014

Past Experience

  • Teacher Leuven, Belgium
    September 2014 --- June 2015

    Teaching anatomy, physiology and pathology

  • Senior Clinical Research Associate (CRA) Brussels, Belgium
    October 2013 --- September 2014

  • Clinical Research Associate (CRA) Brussels, Belgium
    October 2011 --- September 2013

  • Clinical Trial Coordinator (CTC) Brussels, Belgium
    May 2011 --- September 2011

  • Teacher Brussels, Belgium
    September 2010 --- April 2011

    Teacher medical courses (anatomy, physiology, ...)


Self Assessment :
Attention to detailCollaborationCommunicativeCritical thinkingFlexibilityIndependenceProactivityProblem solvingResponsibilitySelf-disciplineTrust


Self Assessment :
Actions and modes of action of human physiologyAnesthesiaBiomedical SciencesCancer ResearchCardiovascular diseasesCell SignalingClinical monitoringClinical researchClinical Trial Management System (CTMS)Good Clinical Practice (GCP)Interpret clinical trial resultsKOL managementMammalian Cell CultureManaging Clinical Trial SuppliesMedical affairsMedical writingOxidative stressPathologyPhase IPhase IIPhase IIIPresentation SkillsPresentationsResearchSearch literature on clinical trialsStandard Operating Procedure (SOP)Pharmaceutical Industry Scientific writingScientific Writing

Skills and Expertise

Self Assessment :
Assure medical quality Create SOPs Guide students Interact with physicians Interact with nurses Monitor a clinical study Interpret data Search literature on clinical trials Use a confocal microscopy Write papersAct as the main line of communication between the sponsor and the investigatorAdminister, maintain and co-ordinate the logistical aspects of clinical trialsAdverse event reportingAdvise on medical perspectivesAdvise on strategyAlzheimerAnswer, transfer and handle incoming calls as needed.Archive study documentsAssess site feasibilityAssist study siteAssist with experimentsAssure medical qualityAttend investigator meetingAttend seminars, courses and meetings within and outside the companyBuild trial master file (TMF)Cell culturecollaborate in research projects at universitiesCollaborate with principal investigatorCollect financial data from hospitalsCommunicate with investigatorConduct close-out visitsConduct literature searchesConduct maintenance visitsConduct research at universitiesConfirm protocol complianceContract approvalcontrol different protocol versions and other essential documentsData verificationDiscuss treatments with investigatorDirect co-workers to achieve resultEnsure good clinical practice (GCP)Interact with ethics committeeInteract with physiciansInteract with nursesLiaise with doctors and other professionals throughout the studyManuscript preparationMonitoring subject compliancePlan experimentsPromotional materialsProvide medical insightsProvide support for scientific and/or technical projectsProvide trainingPublication of articlesRead medical literatureRead medical literature to maintain current awareness and knowledgeResolves queriesResearch at universitiesReview exclusion criteriaReview inclusion criteriaReview study protocolsSchedule sponsor monitoring visitsSchedule trial visitsSearch literature on clinical trialsSerious Adverse Event (SAE) ReconciliationSupervise PhD studentsTeach university studentsTeachingTrain off site staffTrain on site staffTrain StaffUse western blotting techniqueWrite papersProtocol management


  • Ph.D. in doctor of biomedical sciences from K.U. Leuven in 2010
  • Master in Biomedical Sciences from K.U. Leuven in 2004

Training and Certification

  • French course CLT level B2 - vantage in 2014 Certification
  • Seminar the evolutionary path for clinical studies in 2014 Certification
  • Business management in 2013 Certification
  • Certified attendance to clinical research course (K.U. Leuven) in 2011 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Medical Advisor Medical Manager Medical Science Liaison (MSL) Medical Officer Medical Director
  • Work From Home:
  • International:


    Expert has 2 publications (Will be avalible with full profile)

Area / Region

Leuven, Belgium


Driving License
  • Yes