I built applications for Administration & Control, Procurement, HR and Clinical Development departments:among these, a TimeSheet application used by Administration & Control for reporting hours of funded projects and applications for the management of authorization workflows such as Expense Approvals, AFI (Investment Authorizations), Disposal of Company Assets and Purchase Requests.I have also designed software for managing clinical protocols and registration of Drugs.For all these applications I personally take care of user support, drafting documentation as well as of testing and training phases.I am Administrator and Content Manager for both corporate websites and Intranet Portal. I led the deployment project of the intranet portal using the SharePoint 365 platform, Teams, Azure and Project Server as well as the deployment of corporate websites with Joomla / WordPress.I realise and manage high-security data rooms for due diligence and scientific data exchange, where confidenciality is mission critical.

Responsible for development of Regulatory Affairs applications (business analyst, code developer and database designer) .IT Service Manager of Regulatory Affairs applications with worldwide responsibilities.

Computational chemistry: molecular modelling studies (Computer Aided Drug Design).Improuvement of drug profile by means of statistical methods (QSAR).

Team member in R&D projects in the Cardiovascular and Respiratory areas.Responsible for design and synthesis of new molecules - Corporate database design and management (MDL ChemBase - DbIII).