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Summary

Study Leader and Coordinating Data Manager specialized in breast cancer phase II and III studies with 7 years of experience working in a non-profit academic clinical research organisation.

 

Experiences

Current Experience

  • Data Integration Specialist
    Since December 2016

Past Experience

  • Study Leader and Coordinating Data Manager
    March 2012 --- November 2016
    Management of international breast cancer phase II and III clinical trials in collaboration with Pharmaceutical Companies

  • Clinical data manager Brussels, Belgium
    September 2008 --- February 2012
    Ensure an appropriate collection, recording, transmission, validation and correction of clinical data in compliance with the protocol and data management plan for a subset of countries, sites, patients participating in an international breast cancer phase II and III studies.

  • R&D Scientist Namur, Belgium
    October 2006 --- August 2008

  • R&D Scientist
    October 2006 --- August 2008

Personality

Self Assessment :
Attention to detailProactivityOrganizationResult Oriented

Knowledge

Self Assessment :
CRFeCRFOracle ClinicalOncology Clinical ResearchAccessGood Clinical Practice (GCP)CDISCSDTM
LinkedIn Assessment :
Essais cliniquesICH-GCPProtocoleCRFsClinical Data ManagementOracle ClinicalOracle RDCDéveloppement cliniqueCancerGestionnaire de données biomédicalesBreast CancerClinical trialsPostgreSQLMicrosoft AccessInDesignRecherche clinique

Skills and Expertise

Self Assessment :
Review protocolsDesign case record form (CRF)UATURSReview data

Education

  • Specialised Studies in Applied Biological Sciences (DES) in from University of Namur (FUNDP) - Belgium in 2006
  • Master in Biological Science in Molecular and Cellular Biology from University of Namur (FUNDP) - Belgium in 2005

Training and Certification

  • CDISC standards for data managers - ACDM webinar in 2015 Training
  • Principle of IHC GCP - Quintiles Global Learning (e-learning) in 2015 Training
  • Clinical Project Management Course - ECCR in 2013 Training
  • Regulatory Affairs for Clinical Trials - Dr Brown in 2012 Training
  • Organisation and implementation of cancer clinical trials - EORTC in 2011 Training
  • Oncology Lessons - Erasme in 2008 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    French
    Native
    English
    Professional Proficiency
    Dutch
    Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Operations Manager associate Clinical Project Manager Clinical Data Manager (DM)
  • Locations I am interested in:
    Braine-l'Alleud, Belgium Brussels, Belgium Gosselies, Charleroi, Belgium Waterloo, Belgium
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
  • International:
    No

Area / Region

Enghien, Belgium

Others

Driving License
  • Yes