BrightOwl Loader Loading

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 protocol and GLP including the shipment of samples to centralized laboratories - 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

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