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Experiences

Past Experience

  • Clinical Project Manager (CPM) Homebased

    August 2014 --- April 2016
    Change Management

  • Sabbatical year

    August 2013 --- August 2014

  • Clinical Research Specialist Mechelen, Belgium

    April 2011 --- April 2013
    Medical Device

  • Clinical Trial Manager Zaventem, Belgium

    June 2009 --- April 2011
    Data Management

  • Principal Clinical Research Associate Zaventem, Belgium

    June 2007 --- June 2009
    Medical Device

  • Clinical Research Associate (CRA) Zaventem, Belgium

    November 2005 --- June 2007

  • Clinical Research Associate (CRA) Uccle, Belgium

    April 2005 --- November 2005
    Clinical trials

  • Clinical Research Associate (CRA) Braine-l'Alleud, Belgium

    June 2004 --- March 2005
    Clinical trials

  • r&d Assistant Destelbergen, Belgium

    December 2001 --- June 2004
    Phase I

Personality

Self Assessment :
Attention to detailCoordinationCreative thinkingEfficiencyFlexibilityIndependenceInterest in knowledgeKindnessOrganizationProblem solvingResponsibilityResult Oriented

Knowledge

Self Assessment :
R&DAdverse Events (AE)Biomedical SciencesCancer ResearchClinical monitoringClinical operationsClinical researchClinical trial budgetingClinical trial managementClinical Trial Management System (CTMS)CROCRF designData entryData cleaningeCRFInformed Consent ProcessInformed Consent DocumentsInternational Project ManagementMedical DevicesISO 14155ICH-GCP

Education

  • Master in Biomedical Sciences from University of Brussels in 2001

Languages

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

Work Preferences

  • Positions I am interested in:
    Clinical Project Manager (CPM)
  • Work From Home:
    Yes, 3 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl employee :    100% FTE
  • International:
    Yes

Area / Region

Antwerp

Others

Driving License
  • Yes

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