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During my PhD, I worked on a clinical study about possible use of renal markers in cats. I gained experience in clinical studies, data analysis, project management, scientific writing and working in a team. I became interested in pharmaceutical industry, clinical trials in specific, in which I would like to develop my competences in a novel way. Furthermore, I am a team player, very conscientious, communicative, dependable, perseverant and integer, qualities I want to use to obtain my goals. 


Current Experience

  • PhD student Merelbeke, België
    Since October 2010

    Doctoral researcher at Ghent University, Faculty of Veterinary Medicine, Department of Medicine and Clinical Biology of Small Animals

       Clinical Research (renal markers)

       Grant writing, experimental design, data collection, data analysis

       Writing publications (first author of 7 A1 publications)

       Attending Conferences

    Presentations to industry, academia, veterinarians and students of veterinary medicine

       Supervising students with master's theses

       Coaching other veterinarians in research


Self Assessment :
Analytical thinkingAttention to detailDependabilityFlexibilityIndependenceInterest in knowledgeOrganizationSelf-disciplineSociability


Self Assessment :
Scientific writingBiomarkersClinical Data Management (CDM)Clinical operationsClinical Study DesignClinical researchData AnalysisInformed Consent ProcessInterpret clinical trial resultsInterpret clinical trial resultsLaboratory study designMicrosoft ExcelNephrologyPatient Screening and Recruitment

Skills and Expertise

Self Assessment :
Analyze data Create SOPs Develop protocols Develop clinical trial protocols Interpret data Monitor a clinical study Search literature on clinical trials Write papersAnalyze dataAssist with proceduresAssist with experimentsAttend seminarsBiomarker ResearchClinical data collectionConduct literature searchesComplete study proceduresConduct research at universitiesConduct the trialConduct university research Control dataCoordinate with the ethics commiteeDevelop clinical trial protocolsDevelop clinical hypothesesEnsure data consistencyEnsure data integrityEnsure good clinical practice (GCP)Evaluate protocolsInterpret dataManuscript preparationManuscript preparation and reviewManuscript reviewMonitor dataNetworkObtain grantsOral presentationPatient recruitmentPlanning clinical studiesPresent clinical resultsPresent data at congressPublication of articlesPublish scientific projectsRead medical literatureReview exclusion criteriaReview inclusion criteriaScreen patientsSearch literature on clinical trialsSet up a clinical studyWrite papers


  • Master in Veterinary Sciences from Ghent University in 2010

Training and Certification

  • Leadership and Professional Efficiency in 2015 Training
  • Advanced Academic English: Conference Skills-Effective Slide Design in 2014 Training
  • Clinical Studies: Study Design, Implementation and Reporting in 2013 Training
  • Effective Scientific Communication in 2012 Training
  • Statistics: Introductory Statistics. Basics of Statistical Interference in 2014 Certification
  • Laboratory Animal Science in 2012 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Project Leader Clinical Research Associate (CRA) Clinical Research Consultant Clinical Project Manager (CPM) Clinical Research Coordinator Clinical Research Nurse Clinical Research Associate (CRA) Clinical Trial Assistant (CTA) Clinical Laboratory Technician Clinical Operations Manager Clinical Research Manager Clinical Trial Assistant (CTA) Veterinary Clinical Research Sr. Associate
  • Locations I am interested in:
    Antwerpen, België Brussel, België
  • Work From Home:
    Yes, 2 to 5 days per week
  • Work Regime:
    Permanent position :    Permanent% FTE
  • International:


    Expert has 7 publications (Will be avalible with full profile)

Area / Region

Gent, België


Driving License
  • Yes