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master of clinical Biomedical Sciences looking for a challenging job opportunity in Clinical research or the broader biomedical domain, in which i can apply my detail-oriented, social and creative personality.


Past Experience

  • Clinical Research Associate (Junior) Ypres, Belgium

    October 2016 --- March 2017
    • write and provide Training on sops (standard operating procedures)
    • tmf (trial master file) maintenance and Quality Control
    • write monitoring reports
    • write follow-up letters
    • prepare and co-monitor for onsite monitoring (e.g. source data Verification, drug accountability, Investigator file check)
    • prepare and co-monitor for close-out visits
    • prepare ethical commission submission
    • site selection
    • Translation and review of translations of study specific documents (English - dutch)

  • Masterthesis fine discrimination of visceral stimuli in a context of fear conditioning

    September 2015 --- June 2016
    carrying out a Clinical Experiment, reading and writing around the topic of visceral discrimination, working independently.

  • Student job sales woman Roeselare, Belgium

    July 2013 --- August 2015

  • Student Internship

    April 2015 --- April 2015
    uzl department plastic, reconstructive and cosmetic Surgery: working in a Healthcare team, interacting with patients and experiencing the functioning of an Operating Room.

  • Student Internship

    March 2015 --- March 2015
    uzl department Neurology: working in a Healthcare team and interacting with patients.

  • Student Internship

    February 2015 --- February 2015
    uzl department Laboratory Medicine: learning more about all techniques used in the Lab.

  • Student Internship

    November 2014 --- December 2014
    Laboratory of Biological Psychology: working with Laboratory animals and learning about ltp, ltd and brain processes involved in Alzheimer's disease.

  • Student job sales woman Roeselare, Belgium

    July 2011 --- August 2012


Self Assessment :
Creative thinkingCommunicativeCritical thinkingProblem solvingAttention to detailIndependenceKindnessResponsibilityTrustCollaborationCuriosityFlexibilityInterest in knowledgeOrganizationProactivity


Self Assessment :
Biomedical SciencesClinical researchClinical trialsElectrocardiogram (ECG)Good Clinical Practice (GCP)HealthcareHospitalsICH guidelinesInformaticsLaboratory Animal MedicineLife SciencesLifesciencesMetabolismNeurologyNeurosciencePatient recruitmentPhotoshopPlastic surgeryPresentation SkillsProblem SolvingProject PlanningProtocolResearchscienceScientific CommunicationsScientific WritingSearch literature on clinical trialsSocial SkillsSPSSTeamworkTranslational ResearchUnderstanding of regulatory guidelinesUnderstand how results translate to practice
LinkedIn Assessment :
Creative Thinkingteam playerEnglishPhotoshopBiomedical SciencesProblem SolvingAttention to detailsCritical ThinkingMicrosoft OfficeMendeleyClinical researchClinical trialsPatient CareHealthcarescienceLife SciencesICH-GCPResearch

Skills and Expertise

Self Assessment :
Analyze data Interact with nurses Interact with physicians Interpret data Search literature on clinical trials Write papers Write protocolsAlzheimerAssist with experimentscollaborate in research projects at universitiesCollaborate with medical teamCollect dataCommunicate effectively on different company levelsCommunicationConduct animal studiesConduct limited data and/or statistical analysis.Conduct literature searchesConduct research at universitiesConduct studiesConduct the trialConduct university research Coordinate projectsData entryDesign efficiency studyDesign studiesDistribute study documentsEnsure good clinical practice (GCP)Execute scientific projectsGastrointestinal diseasesHandle incidentsInformed consent processInteract with nursesInteract with physiciansInteract with pre-clinical scientistsInterpret dataInterpret research resultsInterpret scientific dataLiaise with research teamLiaise with research team in order to accurately collect and record datalifescienceManage clinical trial files/documentsManage research projectsManage subject consent formObserve trends in dataOperate research equipmentOrganise meetingsOral presentationPatient recruitmentPlan experimentsPlanning clinical studiesPresent clinical resultsproject managementReport study conclusionsSchedule trial visitsSearch literature on clinical trialsSolve problemsStatistical analysisUnderstand protocolsWrite documentsCreate standard operating procedure (SOP)Ethics committee submissionsBuild trial master file (TMF)Manage trial master file (TMF)monitoringFollow up projectsAssess site feasibilitytranslation of study specific documents


  • Master's degree in biomedical sciences in Biomedical Sciences, General from KU Leuven in 2016
  • Bachelor's degree in Biomedische wetenschappen / Biomedical sciences from KU Leuven in 2014
  • in ASO, sciences and mathematics from Barnum (Roeselare) in 2011
  • in from SASK Roeselare in 2011

Training and Certification

  • Good Clinical Practice (GCP) certificate in 2017 Certification
  • Laboratory animal science FELASA B in 0000 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Administrative Assistant associate Clinical Project Manager Biomedical Scientist Clinical Data Architect Clinical Development Consultant Clinical Data Reviewer Clinical Operations Manager Clinical Project Manager (CPM) Clinical Research Coordinator Clinical Research Consultant Clinical Safety Associate Clinical Study Nurse (SN) Clinical Supply Manager Clinical Trial Assistant (CTA) Clinical Trial consultant Clinical Trial Coordinator (CTC) Clinical Trial Manager (CTM) Clinical Trial Specialist (CTS) Data Manager Data Reviewer Data Scientist Data Architect Drug Safety Officer Field Clinical Research Specialist Freelance Science Writer Junior Scientist Medical Affairs Associate Medical Data Coordinator Medical Officer Medical Science Liaison (MSL) Medical translator Medical Writer Pharmacovigilance Assistant Pharmacovigilance Officer QA Officer QA Consultant QC Specialist QC/QA Manager Quality Assurance (QA) Manager Quality manager R&D Assistant R&D Scientist Regulatory and Start-Up Specialist Research Assistant Research associate Research fellow Research Trainee Reviewer Sample Coordinator Scientific Associate Science teacher scientific translator Scientific Writer Scientist Study Start-up Specialist
  • Positions I am NOT interested in:
  • Locations I am interested in:
    Bruges, Belgium East Flanders, Belgium Ghent, Belgium Izegem, Belgium Kortrijk, Belgium Roeselare, Belgium Tielt, Belgium West Flanders, Belgium
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position :    FTE(100%)% FTE
  • International:

Area / Region

Roeselare, Belgium


Driving License
  • Yes

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