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Summary

clinical research experience

  • 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

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: 

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, science)" >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 related professional experience

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

 

 

 

 

 

Knowledge

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

Education

  • Bachelor in Biomedical Sciences from IFTAB in 2015

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
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:
    No

Area / Region

Bruxelles, Belgique

Others

Driving License
  • No

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