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My first experience started at Thermo Fisher Scientifc, where I was employed as Customer Service Specialist.

After my journey within Thermo Fisher Scientific, I started working for USG as a Project Consultant (currently).

Working as a consultant requires a lot of flexibility, the need of adapting yourself to different functions and levels, the ability to learn many different aspects and working in a crossfunctional environment.

My experience is quite diverse and includes working as a Clinical Trials Assistant, Data Manager, Proposal Analyst, Product Developer. More details can be found in my resume.




Current Experience

  • Sales Support/Development Zaventem, België
    Since May 2015

Past Experience

  • Recruitment & Selection Specialist Asse, België
    April 2015 --- June 2015

  • Product Developer Zellik, Asse, België
    September 2014 --- April 2015

  • Proposal Analyst Neder-over-Heembeek, Brussel, België
    September 2013 --- August 2014

  • Clinical Trial Assistant/Data Management Vilvoorde, België
    July 2012 --- September 2013

  • Customer Service Specialst Erembodegem
    October 2011 --- June 2012


Self Assessment :
Analytical thinkingInterest in knowledgeOptimismOrganizationProactivityProblem solvingService orientedSociabilitySelf-disciplineStrategic thinkingTrustWillingness to compromiseIndependenceFlexibilityAssertivenessAttention to detailAuthenticityCharmCollaborationCompetitivenessCoordinationCreative thinkingCritical thinkingCuriosityEfficiencyStriving


Self Assessment :
Clinical researchClinical trial managementClinical trialsCTMSData AnalysisData cleaningData entryData ManagementEnglishGCPGeneral practiceGermanGood Laboratory Practice (GLP)GMPGood Clinical Practice (GCP)Good Manufacturing Practice (GMP)ICH GCP guidelinesCAPAClinical Data Management (CDM)Electronic Data Capture (EDC) ICH-GCPMicrosoft ExcelMicrosoft Officepeople managementPowerPointProblem-solving methods and troubleshootingPrinciples and ethics of clinical researchProduct designProcess improvementProtocolQuality Assurance (QA)QualificationR&DRegistration of the productRegulatory affairsRegulatory RequirementsRegulatory submissionsSerious Adverse Event (SAE)StatisticsStrategic PlanningTeam LeadershipVerification

Skills and Expertise

Self Assessment :
Analyze data Assure medical quality Build and manage the Trial Master File (TMF) Control data Interact with nurses Interact with physicians Interpret data Report data Use content management systemsAdministrative supportAdverse event reportingArchive study documentsAssist with proceduresAssure medical qualityClinical data collectionCollect patient forms and questionnairesCollaborate with project teamCollaborate with principal investigatorComplete case report form (CRF)Conduct the trialCoordinate ethics committeeCoordinate with the ethics commiteeCreate clinical documentsCreate study documentsData analysisData codingData entryData validationData verificationDesign case record form (CRF)Design clinical trialDistribute study documentsDocument adverse eventsDocument data reporting systemsDocument data collection systemDocument employees training requirementsEnsure data consistencyEnsure good clinical practice (GCP)Ethics committee applicationEthics committee submissionsEvaluate impurity identificationEvaluate licensing opportunitiesFollow-up of quality assurance activitiesGeneral office managementGenerate regulatory submissions Handle callsGuide staffImplement data reporting systemsInteract with CROsInteract with ethics committeeInteract with nursesInteract with pharmacistsInteract with physiciansInterpret dataLiaise with doctorslifescienceManage clinical trial files/documentsManage Clinical Trial Management System (CTMS) Manage data collection systemManage data reporting systemsManage subject consent formManage trial master file (TMF)Monitor dataNetworkOffice managementOrganise meetingsPrepare internal auditsPrepare regulatory documentsPreparing referral lettersProtocol managementQuality control processRegulatory documentationRegulatory submissionsReport dataReport serious adverse events (SAE)Report study conclusionsRespond to audit findingsRetrieve study documentsReview medical reportsSearch literature on clinical trialsSolve problemsUse content management systemsValidate dataVerify dataWork under specific instructions


  • Advanced Bachelor in International Business Management from University College Ghent in 2011
  • Bachelor in Office Management from University College Ghent in 2010

Training and Certification

  • People Management in 2014 Certification
  • Project Management in 2014 Certification
  • Barnett - Fundamentals GCP Exam in 2013 Certification


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

Work Preferences

  • Notice Period:
    7 weeks
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position
  • International:

Area / Region

Moerbeke, Geraardsbergen, België


Driving License
  • Yes