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Past Experience

  • Drug Safety Officer Vilvoorde, Belgium

    September 2015 --- January 2016
    • management of post-Marketing safety reports in the area of oncology, Neurology, haematology and Ophthalmology
    • collection, processing, Documentation, routing, and follow-up of spontaneous reports (sr) and solicited Adverse Events (ae) or serious Adverse Events (sae) reports from patient oriented programs (pop), non-interventional studies (nis) and compassionate use programs for assigned novartis products
    • accurate and consistent transcription, translations and Data entry of all safety reports from source documents into the Drug Safety application with emphasis on timeliness and quality
    • general support for the clarification of safety issues: clarification of safety reports and procedures, contacts with investigators when the CRA is not available, contacts with central sites as needed
    • involvement with other local/global Drug Safety associates to ensure accurate evaluation of safety data, provides an interface with the medical and non-medical community
    • exchange of information with other companies
    • responsible for the monitoring and reporting of Patient Safety information
    • contribute to audits, corrective action plan, investigation and Health authority inspections
    • involvement in local rmp implementation, use of targeted follow-up checklists or questionnaires
    • interaction with Quality Assurance for adequate reporting of quality complaints, lack of efficacy reports, and combined safety issues
    • sharing the Drug Safety ward duty as needed, i.e. answering calls on mobile telephone with the free safety line during and out office hours

  • Cancer researcher Ghent, Belgium

    October 2013 --- June 2015


Self Assessment :
Innovative thinkingAttention to detailAdaptabilityAssertivenessCommunicativeCuriosityCritical thinkingEfficiencyFlexibilityOptimismProblem solvingResponsibilityStrategic thinking


Self Assessment :
GeneticsPharmacogeneticsNeurologyNeuroscienceDrug Safety and PharmacovigilanceoncologyOncology Clinical ResearchClinical pharmacologyClinical research Scientific writingScientific CommunicationsPresentation Skills Cell biology

Skills and Expertise

Self Assessment :
geneticsdrug safetyPharmacovigilanceNeuroscience Analytical skills Analyze data Interact with physicians Interpret data Molecular Diagnostics Receptor Pharmacology Write papersAdverse event reportingAttend seminars, courses and meetings within and outside the companyClinical data collectionCollaborate with medical teamConduct university research Data entryDesign clinical presentationDevelop ICH/GCP compliant processesDevelop Quality Risk Management (QRM) initiativesEnsure good clinical practice (GCP)Handle callsInteract with pharmacistsInteract with physiciansInteract with nursesInterpret scientific dataInterpret research resultsLead teamsLiaise with doctors and other professionals throughout the studyLiaise with research teamManage multiple projectsOral presentationOrganize scientific projects (in biology)Present clinical resultsR&DReview medical reportsSerious Adverse Event (SAE) ReconciliationTeach university studentsWrite medical reports


  • Translation in Business and Medical English from Education First language school in 2016
  • Master of science in Biomedical Sciences in Genetics and neurosciences from Ghent University in 2015
  • Bachelor of science in Biomedical Sciences in Biomedical Sciences from Ghent University in 2013

Training and Certification

  • EF Standard English Test (EFSET) - C2 in 2016 Certification
  • Good Clinical Practice - Clinical Studies in 2015 Certification
  • FELASA c (laboratory animal sciences) in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Medical Science Liaison (MSL) Medical Advisor Medical information Medical affairs Drug Safety Drug Safety Officer
  • Locations I am interested in:
    Brussels, Belgium Ghent, Belgium Puurs, Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    80-100% % FTE
  • International:


    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Brussels, Belgium


Driving License
  • Yes

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