Francesco Schievano

Experience

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  Independent

  Jan 2010 - Jan 2017

  Private Tutor for High School students
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  Molecular Modeling Section, Università degli Studi di Padova

  Apr 2016 - Mar 2017

  Master Thesis Student
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  Istituto Oncologico Veneto IOV - IRCCS

  Jun 2018 - Nov 2018

  Pharmacovigilance Intern

  During my tenure as a pharmacovigilance intern, I undertook the following key responsibilities:Conducting thorough screening and analysis of medical records to detect adverse events (AEs).Assessing and promptly reporting suspected adverse drug reactions (ADRs) in compliance with regulatory requirements.Ensuring the proper maintenance and management of the local pharmacovigilance database.

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  Regional Pharmacovigilance Centre of the Region of Veneto - University of Verona

  Dec 2018 - May 2024

  Pharmacovigilance Officer

  As the Assistant to the Head of the Pharmacovigilance Unit at Verona Integrated University Hospital (AOUI), my role encompassed the following duties and responsibilities:Validation and processing of Individual Case Safety Reports (ICSRs) submitted by healthcare professionals within AOUI.Coding adverse drug reactions accurately using MedDRA.Determined and requested pertinent follow-up data for cases to ensure consistency of case entry and high data quality standards.Management of requests from Marketing Authorization Holders (MAHs) related to specific ICSRs.Delivery of pharmacovigilance training to healthcare personnel within AOUI.Preparation of pharmacovigilance reports, including reports on the performance and activities of the pharmacovigilance unit at AOUI.Handling inquiries from AOUI healthcare professionals regarding safety issues associated with specific drugs.As a pharmacovigilance officer at the Regional Pharmacovigilance Centre of the Region of Veneto (CRFVV), I was entrusted with the following key duties and responsibilities:Conducting thorough assessments and analyses of ICSRs stored in the National Pharmacovigilance Database (RNF) as part of our daily pharmacovigilance operations.Assessing potential causal relationships between drug exposure and ADRs based on available data sources.Executing semi-annual signal detection activities to identify potential safety signals.Developing Standard Operating Procedures (SOPs) for internal pharmacovigilance activities.Providing mentorship and guidance to new team members.Collaborating on and actively participating in various pharmacovigilance projects coordinated by the CRFVV. Show less

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  Regional Coordination for Oncological Services - Veneto Institute of Oncology

  Jun 2024 - now

  Compliance Officer

  As a compliance officer at the Regional Coordination for Oncological Services, my responsibilities and tasks include the following:• Developing guidelines and Standard Operating Procedures (SOPs) for the management of oncologic activities.• Contributing to the development of Diagnostic and Therapeutic Care Pathways (DTCPs).• Ensuring compliance with national and international oncology standards.• Regularly monitoring and reviewing patient care practices to identify areas for improvement.• Managing documentation and reporting for compliance purposes.• Implementing training modules for new technologies and treatment methods. Show less