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.
Sales Support/Development Zaventem, België
Since May 2015
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
Analytical thinkingInterest in knowledgeOptimismOrganizationProactivityProblem solvingService orientedSociabilitySelf-disciplineStrategic thinkingTrustWillingness to compromiseIndependenceFlexibilityAssertivenessAttention to detailAuthenticityCharmCollaborationCompetitivenessCoordinationCreative thinkingCritical thinkingCuriosityEfficiencyStriving
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
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