Silvia Cavalli

Silvia Cavalli

Biomedical researcher in the Oncology field

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location of Silvia CavalliLecco, Lombardy, Italy

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  • Timeline

  • About me

    Country Study Manager presso Roche

  • Education

    • OPIS s.r.l.

      2012 - 2012
      CRA training course

      Training on: ICH-GCP, Clinical research methodology, Trial Start-Up, ‘Osservatorio Nazionale sulla sperimentazione clinica dei medicinali’, GMP, Feasibility and Site Selection, Initiation, Monitoring, Close-out, Garante guidelines and ‘Testo unico privacy’, ISO 9001, ISO 27001, Pharmacovigilance, Data Management, eCRF.

    • Liceo Scientifico 'Maria Gaetana Agnesi', Merate (LC), Italy

      2001 - 2006
      Scientific High School Diploma

      Scientific grounding and study of two foreign languages (English and French).

    • Libera Università Vita-Salute San Raffaele

      2009 - 2011
      Second level Degree in Medical, molecular and cellular biotechnology

      Thesis internship carried out in the Division of Molecolar Oncology (Laboratory of 'Preclinical models of tumor') of San Raffaele Scientific Institute. Thesis title: "Role of HIF-1alpha transcriptional factor in Chronic Lymphocytic Leukemia", Supervisor: Prof. Federico Caligaris Cappio, Co-supervisor: Dr. Rosa Bernardi.Grade: 110/110 cum laude.

    • Libera Università Vita-Salute San Raffaele

      2006 - 2009
      First level Degree in Medical and pharmaceutical biotechnology

      Thesis title: "Molecular and clinical features of angiogenesis in hematological malignancies", Supervisor: Prof. Guido Poli, Co-supervisor: Dr. Rosa Bernardi.Grade: 110/110 cum laude.

  • Experience

    • Fondazione Centro San Raffaele del Monte Tabor

      Sept 2010 - Feb 2012
      Biomedical researcher in the Oncology field

      Study of the role of the transcription factor HIF-1alpha in the pathogenesis of Chronic Lymphocytic Leukemia, through in vitro and in vivo experiments, and pre-clinical testing of a new drug for the treatment of different hematological malignancies.

    • OPIS srl

      Feb 2012 - Jul 2012
      Trial Start Up specialist

      Management of ethical and regulatory clinical studies submissions for oncologic clinical trials.

    • OPIS s.r.l.

      Aug 2012 - Sept 2015

      Project management of interventional and international phase I, II and III clinical trials in Hematology and Oncology therapeutic areas. Management and coordination of regulatory clinical trials. Monitoring of interventional and international phase I, II and III clinical trials in Hematology and Oncology therapeutic areas. Management of regulatory clinical trials.Management of all different stages of a clinical trial’s life cycle: feasibility, pre-study, initiation, monitoring and close out.CRA certified according to Italian Decree of 15.11.2011.

      • Project Manager

        Dec 2013 - Sept 2015
      • Clinical Research Associate (CRA)

        Aug 2012 - Dec 2013
    • Roche

      Sept 2015 - now

      Project co-ordination and oversight, operational and management support to Country Study Manager for both global and local clinical trials.

      • Country Study Manager

        Jan 2017 - now
      • Country Study Specialist

        Sept 2015 - Dec 2016
  • Licenses & Certifications

    • DELF Certification (A1, A2, A3, A4)

      Ministère de l'Education Nationale Français
    • ECDL Core (Full)

      CEPIS
    • First Certificate

      University of Cambridge