Damien LE BARILLEC

An analytical & logic-based professional who has extensive SAS experience as well as a broad background in database programming

Advanced SAS programming skills, to support one or more Phase 1- 4 clinical trials, across a variety of medical areas.

Strong mapping knowledge in SDTM format, analysis data set creation in ADaM format based on CDISC implementation guides. TFLs.

Statistical Programmer Denmark (home based) / aug 2022 - dec 2022 Leo pharma account, Ballerup, Denmark Performed programming and quality control of analysis datasets and Tables, Figures and Listings (TFL) for an Integrated Safety Summary analysis for eczema indication, considering multiple pool definitions from several studies. 

Clinical/Statisical Programmer France /Germany (home based) / jan 2021 - jul 2022 
 Programmed data management clinical reports, protocol deviations, AEs reconciliations 
 SDTM and ADAM mapping (specifications and programming) for Excelya Germany 
 Recruitment of SAS Programmers for Excelya in India. 

Clinical Data Programmer France / jan - dec 2020 Sanofi account: Chilly-Mazarin, France 
 Developed and validate standard tables and listings. 
 Programmed protocol deviations for several studies: respiratory, virology & immuno-inflammatory. 

Controlled Terminology Data Steward France / jan - dec 2019 Sanofi account: Chilly-Mazarin, France 

 Managed study requests for Controlled Terminologies (CT) new terms implementation. 
 Managed global requests for implementation of new Sanofi release for CT. 
 Delivered new terms for CT.Conducted weekly Quality Control for CT files to be loaded. 
 Supervised and assure emergencies at study levels and arbitrations. 
 Controlled the evolution of QC process on CT. 

Statistical Programmer Belgium (remote) / nov 2016 - dec 2018 GSK vaccines account: Wavre, Belgium 

 Analysed five studies on Malaria vaccine: Safety/efficacy analysis, immunogenicity and demography. 
 Created analysis data sets (CDISC ADaM and GSK standards). 
 Generated Tables Listings and Figures with SAS (SAS Drug Development). 
 Performed programs Quality Control by code review, edit checks or double programming. 
 Implemented statistical analysis plan protocol in concert with the trial team statistician. 
 Edited Table Figures and Listings table of contents document (Shell) creation. 
 Conducted Statistical Analysis Pooling: Data Safety Update Reports (DSUR) and Investigator Brochures (IB). 
 Submission: created packages for e-submission, produced SAS program, compared analysis tables with clinical study report, create XPT files. 

SAS Developer France / jan 2011 - oct 2016 Servier account: Suresnes, France 
 Supervised and guaranteed the development, optimization, migration and support for SAS applications. 
 Management of resources allocated by development, onboarding of newcomers. 
 Lead and conducted meetings and trainings for internal and external teams (>10 people). 
 Ensured applications validation within Unit Tests managed by SAS programs. 
 Developed Application Web interface using SAS Web stored processes, HTML and JavaScript. 
 Managed development through pair programming and progressively AGILE method implementation. 
 Performed migration of reporting of individual data to SDTM model (minimal standard database, oncology and neuropsychology standards, among others). 

SAS Developer France / jan 2008 - dec 2010 IPSEN account: Les Ulis, France 
 SAS development, design and implementation of scripts for evolutions qualification of a SAS application for the management of a Data Warehouse. 
 SAS data mapping corresponding to standard data model IPSEN. 
 Reports creation within SAS for data review, development and set-up of standards reports, development of a SAS Base application for integrating reports into a host application (Integrated Review). 

Data Manager France / 2000 - 2007 Bayer, Aventis & Sanofi-Synthelabo accounts, France 

 Data management for the following therapeutic areas: Oncology, Internal Medicine, Thrombosis and Infectiology for phase I to IV clinical studies. 
 Lead data manager on studies of phase 2 and 3, representation of data management in study team meetings

2000 IUT of Vannes, France 

University Degree in Technology, Statistics and Data Processing (DUT S.T.I.D)