For Statistical Programmer (SAS ADAM/TLF):
.Professional with experience in Statistical Programming in clinical domain
.Experience and understanding of ICH GCP principles and clinical drug development process
.Good knowledge of CDISC SDTM and ADaM standards
.2 to 10 years of experience in programming related activities for clinical studies (Phase I to IV) and publication
.Advance knowledge of Base SAS, SAS / STAT, SAS /Graph modules and SAS Macros
For SAS SDTM Programmer:
.Hands-on experience on CRF annotation with SDTM mapping
.Ability to identify data issues that affect programming decisions or the integrity of results
For SAS R Programmers:
.Tools: R, Python and SAS programming experience.
.Analytical skills
.Good communication
.Decision making and interpretations.
.Good understanding of statistical models / concepts
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