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Caroline BIDON

ST GERMAIN EN LAYE

En résumé

Pas de description

Entreprises

  • Biotechnology society - Medical writer

    maintenant Responsible for the writing of the study documents from the protocol to the Clinical Study Reports in the oncology and inflammatory disease fields

    Medical writing activities for preparing and submit protocols to AFSSAPS and Ethics Committee for clinical trials on medicinal products, and responses to health authorities questions
  • ABSCIENCE

    maintenant
  • LFB - Medical writer

    2008 - 2010 Experience working on CTD regulatory documents, especially in pediatrics, in the fields of immunology and homeostasis
    Wrote Pediatric Investigation Plans for new medicine according to European regulation, clinical overview and summary
  • ADDS - Clinical Research Associate

    2008 - 2008 Involved in the whole clinical study process, from protocol preparation to clinical trial monitoring, in a broad range of research fields.

    Provided input in writing documents (epidemiology reports, protocols)
    Ensure the monitoring of phase III clinical trials in oncology, neurology and neuropsychology
  • CNRS-BEAUFOUR IPSEN - Doctoral Researcher

    2003 - 2007 Developed experimental and functional analysis methods to allow the use of microarray technology, in collaboration with Beaufour Ipsen company.

    Research Subject : sarcopenia and the effect of a Ginkgo Biloba extract on striated muscle gene expression

Formations

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