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  • QA Auditor – ZOETIS (Formerly Pfizer Animals Health) - Zaventem, Belgium (2016 - present)

Part of the Veterinary Medicine Research Development and Global Quality and Compliance Unit, my main tasks were to:

  • Audit pre-Clinical and Clinical Studies according to VICH-GCPs
  • Provide QA support to the EU clinical development team
  • Participation in a variety of QA-related activities including staff and project meetings, non-study document reviews
  • Clinical Study Coordinator – HUDERF (Queen Fabiola Children’s University Hospital - Brussels, Belgium (January 2013 - May 2015)

My main task involves coordinating the pediatrics clinical trials sponsored by pharmaceutical laboratories and academics in the research areas of hemato-oncology, neurology, diabetology, rheumatology, gastroenterology and Infectiology (Clinical Trials phase Ib - IV):

  • Resources Database Expert - INSERM (French National Institute for Medical Research) Orphanet - Paris, France (2012-2013)

Orphanet is the reference portal for information on rare diseases and orphan drugs. My main tasks were to: 

  • Identify the sources of information on diagnostic tests, on-going research projects from basic research to clinical trials, registries and biobanks
  • Validate the collected data by national teams (40 countries) in the Orphanet databaseClinical Research Associate Coordinator - INSERM CIE802- Martinique, French West Indies (2008-2011)

The Clinical Investigation Center (CIC) is specialized in infectious, emerging and genetic diseases in tropical areas. My main responsibilities involved:

  • Management of prospective multi-center studies in genetics and infectious diseases (HIV, dengue virus, hepatitis B, HPV…)
  • Support to investigators and supporting patients’ recruitments, CRFs and eCRFs filling, SAEs reporting and follow-up
  • Project development and start up process including study organization with the principal investigator, protocol and regulatory documents review and regulatory submissions (Afssaps, ethics committee, CNIL, CPPRB)
  • Coordination of monitoring including team training, trip reports and correspondence review, planning supervision, site issues resolution
  • Acting as reference point for the Biological Resource Center (biobank) of Martinique (CeRBiM)
  • Participation in the expert committee on infectious diseases of Martinique (CEMIE)

Clinical Research Associate - INSERM SC10 - Paris, France (2006-2008)

Inserm SC10 ensures the design, the methodology, the implementation and statistical analysis of scientific studies

  • Management of multi-center studies in the research field of HIV (Phase III and IV) sponsored by the French AIDS Agency
  • Oversight of all aspects of biomedical research: design of protocols, data collection forms and patient information
  • Monitoring activity: Initiation visits, monitoring visits, close-out visits, tracking of patient enrolment and CRFs, management of SAEs, interactions with data management for data clarifications

Clinical Research Associate - INSERM CIE5 - Paris, France (2005)

  • Creation, maintenance, and use of a clinical database on congenital hypothyroidism (PHRC 2005)
  • Data clarifications and database cleaning
  • Tracking of patient enrolment and monitoring visits


Laboratory Technologist (2003 – 2005)

Parasitology and Mycology Laboratory - Hôpital Universitaire Tenon (AP-HP) - Paris, France

  • Acting as head laboratory technologist (reagent kits, staff management and planning)
  • Responsible for parasitology and mycology sectors: culture, identification, serology, MIC determination
  • Responsible for IT and quality assurance for the laboratory
  • Laboratory Technologist (2000 – 2003)

Haematology, Immunology and Hemostasis Laboratory - Hôpital Rothschild (AP-HP) - Paris, France

  • Responsible for cytology and hemostasis sectors
  • Support to the biochemistry laboratory (serology and molecular biology sector)
  • Responsible for the genetics testing related to hemostasis and thrombophilia (MTHFR gene, factor V Leiden, factor II mutation)
  • Processing the biological samples related to the clinical trials conducted on site, including the shipment of samples to central laboratories
  • Responsible for IT in the laboratory







Self Assessment :
Labtechnician Cell biology R&DClinical researchGenetics

Skills and Expertise

Self Assessment :
labManage laboratory procedures Develop clinical trial protocols Monitor a clinical studyClinical data collectionDesign clinical trial


  • Bachelor in Biomedical Sciences from IFTAB in 2015


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Laboratory Technician Lab Technician Clinical Research Coordinator
  • Locations I am interested in:
    Brussels, Belgio
  • Work From Home:
    Yes, 0 to 2 days per week
  • Work Regime:
    Permanent position
  • International:

Area / Region

Bruxelles, Belgique


Driving License
  • No