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Summary

Clinical research experience • CRA / study Coordinator - queen fabiola children's University Hospital (huderf) - brussels, belgium (january 2013-present) my main task involves coordinating the Pediatrics Clinical trials conducted at huderf in Clinical trials Phase II, iii and iv in the research areas of hemato-oncology, Neurology, Gastroenterology, infectiology: - timeline tracking, reports to sponsor and overall management of clinical site (information and consent form, case report forms and e-crfs filling, saes reporting and follow-up) - support to investigators and supporting subjects’ recruitment including vitals signs and eeg assessment - Biological samples processing according to science)" >Protocol and glp including the shipment of samples to centralized laboratories - science)" >Protocol and regulatory documents review and regulatory submissions for the studies sponsored by huderf • information Scientist - Expert resources database – orphanet - inserm (French national institute for Medical Research) - 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 database laboratory related professional experience • acting as head Medical Laboratory Technologist (2003 – 2005) laboratory for parasitology and mycology - hôpital tenon (ap-hp) - paris, france • Medical Laboratory Technologist (2000 – 2003) laboratory for Hematology, Immunology, hemostasis - hôpital rothschild (ap-hp) - paris, france

Experiences

Current Experience

  • Clinical Research Nurse


    Since January 2013
    study Coordinator – huderf (queen fabiola children's University Hospital - management of Pediatrics studies (Phase II, iii, iv): support to investigators & supporting patients’ recruitments (checking inclusion/exclusion criteria), crfs and e-crfs filling, saes reporting and follow-up Study Coordinator – HUDERF (Queen Fabiola Children's University Hospital - Management of pediatrics studies (Phase II, III, IV): Support to investigators & supporting patients’ recruitments (checking inclusion/exclusion criteria), CRFs and e-CRFs filling, SAEs reporting and follow-up

Past Experience

  • Information Scientist

    January 2012 --- January 2013
    orphanet is the reference portal for information on rare diseases and orphan drugs. orphanet is led by a european consortium of around 40 countries, coordinated by the French team. - identify the sources of information on Expert centres, Diagnostic tests, on-going research projects, from basic research to Clinical research, registries and biobanks - enter the data in the orphanet database and validate the collected data by national teams

  • Clinical Reserach Associate Senior

    August 2008 --- August 2011

  • Clinical Research Associate (CRA)

    January 2006 --- January 2008

  • Clinical Research Associate (CRA)

    January 2006 --- January 2006

Knowledge

LinkedIn Assessment :
Clinical researchClinical monitoringHematologyVirologyLaboratory SkillsBiologyGCPsGLPIATAData ManagementEssais cliniques

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Molecular Diagnostics Interact with physicians Control data Lab scale batches Monitor a clinical study Build and manage the Trial Master File (TMF)

Education

  • in Data Management from ClinSight in 2009
  • University degree in Virology from Université Denis Diderot (Paris VII) / University Paris VII in 2008
  • Bachelor's degree in Biomedical/Medical from IFTAB in 1999

Training and Certification

  • Good Clinical Practice in 2015 Certification
  • IATA and dangerous goods regulation in 2015 Certification

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Laboratory Technician Clinical Research Nurse Lab Technician
  • Locations I am interested in:
    Bruxelles, Belgique
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Bruxelles, Belgique

Others

Driving License
  • No

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