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Proven expertise in clinical research, medical information and scientific education. Driven by evidence based medicine and scientific developments. One of my strenghts is transferring complex scientific information in a clear, understandable language. Pro-activity, accuracy and a customer-minded attitude allow me to meet requested deadlines. I am open to short- or long-term assignments where I can offer my accumulated experience to customers searching for a scientific support of their projects.


Past Experience

  • Medical Science Liaison Immunology
    May 2011 --- October 2014
    - Medical point of contact for delivery of accurate scientific information on clinical trials and therapeutic strategies in immunology. - Liaison with health care professionals and academic researchers to discuss new developments. - Organisation of a multi-disciplinary congress. - Development and delivery of scientific courses for clinical operations, sales & marketing teams, external customers.

  • Medical Science Liaison (MSL)
    July 2010 --- June 2011

  • Medical Information Manager Benelux
    May 2001 --- December 2006
    - Central point of contact for questions and quality complaints about any drug from Schering-Plough’s portfolio. - Responsible for the accuracy of all promotional materials. - Creation of a cross-functional workgroup to increase the efficacy of Medical Information Services

  • Quality Assurance Manager Benelux
    December 1999 --- April 2001
    - Responsible for Quality Assurance of clinical trials. - Performing internal and external audits. - Development of Standard Operating Procedures.

  • Clinical Research Associate (CRA)
    February 1997 --- November 1999
    Coordination and monitoring of Phase II/III trials.


Self Assessment :
Analytical thinkingIndependenceDiligenceInterest in knowledgeService orientedProactivityEfficiencyCollaborationAttention to detailFlexibility


Self Assessment :
molecular biologyPeptides
LinkedIn Assessment :
ImmunologyPharmaceutical IndustryMedical affairsClinical researchClinical trialsTherapeutic AreasBiotechnologyGCPClinical DevelopmentRheumatologyMedical InformationGastroenterologyMedical Education

Skills and Expertise

Self Assessment :
analyticManuscript preparation and reviewAdvise on medical perspectivesPresent clinical resultsParticipate in medical reviewOral presentationInteract with physiciansInteract with pharmacistsDevelopment of Pharmacy manualData verificationCoordinate regular advisory board Search literature on clinical trialsProvide training


  • Postgraduate Forensic Research in from Erasmushogeschool Brussel in 2014
  • Postgraduat Toxicologie industrielle in from Université catholique de Louvain in 1996
  • Master in Pharmaceutical Sciences in from KU Leuven in 1995


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

Work Preferences

  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    BrightOwl freelancer :    20 Hours per week
  • International:

Area / Region

Brussel, België


Driving License
  • Yes