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Summary

over the years i have gained a broad experience in Clinical trials, thus becoming a truly all-round Clinical Research Professional. i have managed all types of projects: from small phase 1 trials to large global, phase iiib, full-service programs, as well as Investigator initiated trials. i have worked in several indications, but mostly cardiovascular. besides project- and line-management i have experience with many other aspects of clinical research such as: in-Hospital trial coordination, site selection and start up, regulatory submissions, contracts & Budgets, on-site monitoring, science)" >Protocol & SOP development, database development, CRA Training and Coaching. currently i 'm available for new projects, so if you need support on any task, please contact me on vlietria@gmail.com

Experiences

Current Experience

  • Consultant Clinical Operations


    Since May 2014

  • Owner


    Since March 2014
    Clinical research consultancy Clinical Research Consultancy

  • Project Manager


    Since May 2011
    Project Manager of multi-center, international, Investigator initiated trials Project Manager of multi-center, international, investigator initiated trials

Past Experience

  • Global Project Leader

    January 2007 --- April 2011

  • Head Clinical Research Coordination

    January 2000 --- January 2007

Knowledge

LinkedIn Assessment :
Clinical monitoringGCPCROCTMSClinical trialsPharmaceutical IndustryICH-GCPEDCTherapeutic AreasRegulatory submissionsClinical researchTrial ManagementClinical operationsClinical Data ManagementInfectious diseasesClinical DevelopmentPatient recruitmentPharmacovigilanceCardiologyProtocoloncology

Area / Region

Netherlands

Others

Driving License
  • No

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