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Current Experience

  • Principal Medical Writing Scientist

    Beerse, Belgium
    Since January 2015

    writing of several types of regulatory documents withing the therapeutic area of Infectious diseases.

    Writing of several types of regulatory documents withing the therapeutic area of infectious diseases.

Past Experience

  • Senior Medical Information Manager Lier, Belgium

    April 2008 --- December 2014


    main responsibilities


    ·         perform medical copywriting of congress abstracts, posters, oral Presentations, full manuscripts, educational booklets, slide resources, faqs, congress reports, meeting minutes, Clinical study reports, educational websites, cme questions, etc.


    ·         participate in the coordination and management of symposia and advisory board meetings and in client meetings


    ·         give Presentations during advisory board meetings


    ·         give input for the development of new medical Communication services




    main Therapeutic Areas


    ·         oncology

    ·         Infectious diseases

    ·         Neurology

    ·         orphan diseases

    ·         urology

    ·         Immunology


  • PhD student Leuven, Belgium

    February 2002 --- April 2008

    project:       subcellular localisation and trafficking of the gamma-secretase components

                        (Cell biology of alzheimer’s disease; promotor:  prof. dr. wim annaert)

  • Scientific coworker Antwerpen, Belgium

    August 2001 --- January 2002

    department of Microbiology: Research project about the relationship between macrolide resistance and invasivity for group a streptococci


Self Assessment :
Analytical thinkingAttention to detailCreative thinkingCritical thinkingIndependenceInterest in knowledgeProactivityProblem solvingTrust


Self Assessment :
Cell biology R&D Scientific writingCancerClinical researchClinical study reportsClinical trialsEnglishInfectious diseasesKOL managementMedical oncology Medical writingNeuroscienceoncologyPhases of clinical development (phase I to IV)PowerPointScientific WritingSearch literature on clinical trialsUrology

Skills and Expertise

Self Assessment :
Interpret data Search literature on clinical trials Write papersCollaborate with medical teamCollaborate with project team


  • PhD in Biomedical Sciences from Catholic University of Leuven in 2009
  • Master in Biochemistry from University of Antwerp in 2001
  • Bachelor in Biomedical Sciences from University of Antwerp in 1999

Training and Certification

  • • Statistical thinking for non-statisticians in drug regulation, RK Statistics, UK in 2012 Training
  • • Pharmacokinetics, Leiden/Amsterdam Centre for Drug Research, Holland in 2010 Training
  • • Time management, Kluwer, Belgium in 2010 Training
  • • Successful medical writing, Management Forum, London, UK in 2009 Training
  • • Targeting your audience – Creating an impact with posters – Conference in 2009 Training
  • • Writing for the internet, AG Consult, Belgium in 2009 Training
  • • Effective writing for biomedical professionals, University of Oxford, UK in 2008 Training
  • • Introduction to drug development, Rostrum, London, UK in 2008 Training
  • Languages

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

Work Preferences

  • Work From Home:
  • International:

Area / Region



Driving License
  • Yes

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