Guillaume Abgrall

Having worked in the pharmaceutical industry for over 10 years, I am a Lead Statistical Programmer with considerable experience of leading programming activities across multiple trials in various therapeutic areas (oncology, hematology and pulmonary diseases). I have broad knowledges in metadata, SDTM and ADaM implementation, e-submissions to FDA, development of macros, and study management. In addition to project assignments, I am involved in company initiatives such as development of tools regarding CDISC standards, and more recently we started to build out data standards and platforms for Digital Health. Hands-on experience in pharma companies as Lead statistical programmer ▫️Very strong knowledge of programming and reporting with SAS and R. Strong knowledge of SQL. ▫️Strong ability to implement the latest CDISC SDTM, ADaM, and Define standards. ▫️Statistics: estimation, testing, analysis of variance, linear and logistic regression, survival analysis and simulation. ▫️Flexible, fast, and reactive.