Requirements:
, , or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields
Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group
At least years of Clinical trials related work experience in SAS programming, analysis and reporting in the context of drug development projects is required
Well experienced in Pinnacle validation process, generating define xml using Pinnacle
Extensive experience in implementing CDISC standards, as well as annotating CRFs, creating specifications for SDTM and ADaM datasets
Experienced in creating and the corresponding Reviewers' Guide for SDTM and ADaM datasets
Good verbal and written communications skills in English
Demonstrated knowledge of clinical...