
Silvia Cavalli
Biomedical researcher in the Oncology field

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About me
Country Study Manager presso Roche
Education

OPIS s.r.l.
2012 - 2012CRA training courseTraining 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 - 2006Scientific High School DiplomaScientific grounding and study of two foreign languages (English and French).

Libera Università Vita-Salute San Raffaele
2009 - 2011Second level Degree in Medical, molecular and cellular biotechnologyThesis 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 - 2009First level Degree in Medical and pharmaceutical biotechnologyThesis 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 2012Biomedical researcher in the Oncology fieldStudy 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 2012Trial Start Up specialistManagement of ethical and regulatory clinical studies submissions for oncologic clinical trials.

OPIS s.r.l.
Aug 2012 - Sept 2015Project 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 2015Clinical Research Associate (CRA)
Aug 2012 - Dec 2013

Roche
Sept 2015 - nowProject co-ordination and oversight, operational and management support to Country Study Manager for both global and local clinical trials.
Country Study Manager
Jan 2017 - nowCountry 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
Languages
- itItaliano
- inInglese
- frFrancese
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