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Work Background
Regulatory Affairs Project Manager
VDATARegulatory Affairs Project Manager
Apr. 2024Milan, Lombardy, ItalyRegulatory Affairs and Compliance Manager
Regulatory Affairs and Information Specialist
IBSA GroupRegulatory Affairs and Information Specialist
Nov. 2018 - Dec. 2024SwitzerlandIDMP Implementation Project Lead. Advanced Knowledge of processes and regulatory information managment (Veeva RIM suite System). Advanced knowledge of xEVMPD. Advanced knowledge of Drug Track database (Lorenz). Advance knowledge of eSubmissions (Veeva Pubblishing and eCTD Manager). SPOR User Management, Local HA tools as MHRA, SwissMedic ect.
Regulatory Affairs Specialist
IBSA ItalyRegulatory Affairs Specialist
Dec. 2017 - Nov. 2018Lodi Area, Italy• Managed EudraVigilance data entry and updates for products via xEVMPD, ensuring regulatory compliance. • Utilized advanced knowledge of Lorenz drug track regulatory database for data enrichment and entry. • Collaborated with cross-functional teams to streamline regulatory processes and improve efficiency.
Drug Safety Officer
LifeBeeDrug Safety Officer
Sep. 2017 - Nov. 2017Milan Area, ItalyPharmacovigilance advisor for different companies using Argus Software for adverse events management
Pharmacovigilance Advisor
LifeBeePharmacovigilance Advisor
Jun. 2016 - Aug. 2016Milan Area, ItalyPharmacovigilance advisor for different companies using Argus Software for adverse events management
Research Fellowship
IFOM, the FIRC Institute for Molecular OncologyResearch Fellowship
Sep. 2012 - Jul. 2013Milan Area, ItalyTitle: "Genomic Characterization of DNA:RNA hybrids in S.cerevisiae".
Research Fellow
IFOM, the FIRC Institute for Molecular OncologyResearch Fellow
Nov. 2009 - Jan. 2010Milan Area, ItalyTitle: "Characterization of CISPLATIN sensitive mutants in Yeast".

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