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Directs the technical and operational aspects of study site start up deliverables across countries. Works with major functional area leads (project management, clinical management, legal and regulatory) to identify, evaluate, coordinate and oversee fundamental issues pertaining to the successful site start-up of the project. Provides accurate projections, reports, updates and ongoing risk assessments. Accountable for achieving the final study start-up deliverable (usually projected site activations) within the time period specified in the contract with the Customer. Manages all clinical aspects of allocated studies. Serves as the primary start-up contact for the Project Manager and client.


Current Experience

  • Principal Team Manager - Site Intelligence & Activation
    Since May 2014
    Leads and manages site start-up portion of assigned projects from feasibility trough site activation.

Past Experience

  • Senior Team Manager – Site Intelligence & Activation
    April 2013 --- May 2014
    Leads and manages site start-up portion of assigned project.

  • Principal Clinical Team Manager
    April 2010 --- April 2013
    Responsible for the co-ordination and management of all clinical operations project team members on an international basis (particularly CRA’s), within designated projects.

  • Senior Clinical Team Manager
    January 2007 --- April 2010

  • Clinical Team Manager
    January 2005 --- January 2007

  • Senior Clinical Research Associate (CRA)
    April 2002 --- January 2005

  • Clinical Research Associate (CRA)
    September 1999 --- March 2002


LinkedIn Assessment :
EDCClinical trial managementCROClinical trialsClinical monitoringGCPClinical researchPhase IOncology Clinical ResearchInfectious diseasesRespiratory DiseaseCTMSICH-GCPTherapeutic AreasClinical DevelopmentClinical operationsClinical Data ManagementRegulatory submissionsoncologyOracle ClinicalSOPRegulatory affairsTrial ManagementPharmaceutical IndustryVaccinesProtocolNeurologyPharmacovigilanceRegulatory RequirementsPatient recruitmentFDA


  • Master in Environmental Technology from University of Leuven in 1992
  • Master in Industrial Engineer from Groep T - Internationale Hogeschool Leuven in 1991

Work Preferences

  • Locations I am interested in:
  • Work From Home:
    Yes, 5 Days
  • Work Regime:
    Permanent position
  • International:

Area / Region

Brussels, Belgium


Driving License
  • No