Audrey Goupil

Audrey Goupil

Production Operator

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location of Audrey GoupilLausanne, Vaud, Switzerland

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  • Timeline

  • About me

    Research coordinator at CHUV | Lausanne university hospital

  • Education

    • Gymnase de Morges

      2007 - 2010
      Maturité Fédérale and Baccalauréat (High School Degree)
    • Ecole polytechnique fédérale de Lausanne

      2014 - 2016
      Engineer's Degree Life Sciences and Technologies 5.29/6

      Activities and Societies: Mountain Club

    • Ecole polytechnique fédérale de Lausanne

      2011 - 2014
      Bachelor's Degree Life Sciences and Technologies
  • Experience

    • Nagra

      Jul 2013 - Sept 2013
      Production Operator

      production of smart cards, quality control, maintenance

    • Imina Technologies SA

      Oct 2013 - Nov 2015
      Student Assistant

      production, administration

    • MindMaze

      Jul 2014 - Sept 2014
      Engineering Intern Student

      “Role of person perspective and visual feedback in virtual reality for rehabilitation exercises”. Management of multiple research projects: experimental design, participants recruitment, implementation, data analysis, presentation of results

    • CHUV | Lausanne university hospital

      Feb 2016 - Aug 2016
      Master Thesis Student

      "Interaction between oxidative stress and inflammation in peripheral blood mononuclear cells of schizophrenia patients". Main lab methods used: suspension cell culture, protein extraction, ELISA, Western Blot.

    • CHUV | Lausanne university hospital

      Jan 2017 - Jan 2017
      Laboratory assistant
    • UCB

      Feb 2017 - Jan 2019
      Associate scientist in biopharmaceutics

      Development of biopharmaceutical tools for the support of preclinical and clinical formulation of new chemical entities/small molecules. Main tasks:- in vitro dissolution and absorption assays- mechanistic absorption/PBPK modelling

    • CHUV / Centre hospitalier universitaire vaudois

      Oct 2019 - now

      Coordination of projects involving collection of clinical data and/or biological samples for research purposes (according to the Human Research Ordinance), including:- Development of regulatory and operational documents, research protocol and informed consent.- Submission to the Ethics Committee.- Training of study-staff.- Creation of the clinical database and data entry.- Coordination of patients/participants recruitment, visits, and follow-up. - Translational research:Development of regulatory documents, including research protocol and informed consent.Submission to the Ethics Committee.- Clinical trials:Regulatory support for clinical study coordinators, including preparation of regulatory submission dossier for sponsors, regulatory follow-up of amendments, regulatory maintenance of the Investigator Site File.

      • Translational Research Coordinator

        Aug 2024 - now
      • Regulatory Affairs Officer - Translational and Clinical Research

        Oct 2019 - Jul 2024
  • Licenses & Certifications

    • Good Clinical Practices

      TRREE
      Oct 2019
    • Training and Resources in Research Ethics Evaluation

      TRREE
      Sept 2014
      View certificate certificate
    • Lean Six Sigma Yellow Belt Certification

      UCB
      Feb 2018
    • GastroPlus PBPK Modeling workshop

      Simulations Plus, Inc.
      Mar 2018
  • Volunteer Experience

    • Accompanist for disabled people

      Issued by Association Cerebral Vaud on May 2015
      Association Cerebral VaudAssociated with Audrey Goupil