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Personal Information
Organization / Workplace
Switzerland Switzerland
Occupation
Director, Clinical Data Standard and Data submission at Cytel Inc
Industry
Medical / Health Care / Pharmaceuticals
About
I have more than 20 years of experience in the field of Clinical Research in the area of data-management and statistical programming with different roles in Academic Organisation, CRO and Pharmaceutical Industry, in Italy, Switzerland and UK. I have strong expertise in SAS programming and CDISC standards (mainly SDTM and ADaM). My core expertise is Oncology from phase I to phase IV; in the past I also had experience in Cardiovascular and Intensive Care therapeutic area. While working for Academic Organisation I had also the possibility to conduct epidemiology studies and systematic review of literature data (meta-analysis). As head of a data management team I also led the computer sy...
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Presentations(15)Ìý

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The application of STDM in a no-profit and disease specific organisation - CDISC Italian User Group, Milan (Italy), 2008
The application of STDM in a no-profit and disease specific organisation - CDISC Italian User Group, Milan (Italy), 2008The application of STDM in a no-profit and disease specific organisation - CDISC Italian User Group, Milan (Italy), 2008
The application of STDM in a no-profit and disease specific organisation - CDISC Italian User Group, Milan (Italy), 2008
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From Local Laboratory to Standardisation and beyond Applying a common grading system
From Local Laboratory to Standardisation and beyond Applying a common grading systemFrom Local Laboratory to Standardisation and beyond Applying a common grading system
From Local Laboratory to Standardisation and beyond Applying a common grading system
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Web-Triage An Application for patient registration in phase I dose escalation studies
Web-Triage An Application for patient registration in phase I dose escalation studiesWeb-Triage An Application for patient registration in phase I dose escalation studies
Web-Triage An Application for patient registration in phase I dose escalation studies
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Documents(7)Ìý

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A gentle introduction to meta-analysis
A gentle introduction to meta-analysisA gentle introduction to meta-analysis
A gentle introduction to meta-analysis
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A gentle introduction to survival analysis
A gentle introduction to survival analysisA gentle introduction to survival analysis
A gentle introduction to survival analysis
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Efficacy endpoints in Oncology
Efficacy endpoints in OncologyEfficacy endpoints in Oncology
Efficacy endpoints in Oncology
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