1. Lead the programming activities for a trial, early phase project, or publication activities;2. Maintain efficient interfaces with internal and external customers with support of SR management and the Statistician.3. Develop and comply with project / study standards and specifications following internal and regulatory guidelines.4. Make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, (e)CRF and data… Show more 1. Lead the programming activities for a trial, early phase project, or publication activities;2. Maintain efficient interfaces with internal and external customers with support of SR management and the Statistician.3. Develop and comply with project / study standards and specifications following internal and regulatory guidelines.4. Make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, (e)CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.5. Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for ISS and ISE with high quality and within milestones.6. In consultation with the Statistician, develop specifications for analysis datasets, pooled datasets, and listings. Show less

1. Lead the programming activities for a trial, early phase project, or publication activities;2. Maintain efficient interfaces with internal and external customers with support of SR management and the Statistician.3. Develop and comply with project / study standards and specifications following internal and regulatory guidelines.4. Make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, (e)CRF and data… Show more 1. Lead the programming activities for a trial, early phase project, or publication activities;2. Maintain efficient interfaces with internal and external customers with support of SR management and the Statistician.3. Develop and comply with project / study standards and specifications following internal and regulatory guidelines.4. Make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, (e)CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.5. Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for ISS and ISE with high quality and within milestones.6. In consultation with the Statistician, develop specifications for analysis datasets, pooled datasets, and listings. Show less

Design and / or review database structure Generate and manage Queries Create derived-analysis datasets Act as programmer to produce tables, listings, and figures for the clinical study report Act as programmer to validate SAS programs that produce derived-analysis datasets and data analyses

C#.NET and ASP.NET analyst and Software developer of regulatory systems in GSK for AD HOC sistemi (Mantova, Italy). I have been involved in the development of .NET projects (especially Web applications) in C# language supporting the AJAX technique

I worked as software developer for Euris Solutions., a company that works in Information Technology Market. I was involved in development and maintenance of software.• VB6, C++,/SQL server, Oracle for banking sector (Finmatica Group)• ASP.NET, C#.NET/SQL Server (Quercia Software – Unicredit Group), for tax sector