CHANDRAWAR IT TECHNOLOGIES PVT LTD is seeking a skilled SAS programmer to support clinical trial data programming and reporting in a regulated environment. The role focuses on developing, validating, and maintaining SAS programs, creating TLFs, and contributing to CDISC-compliant SDTM/ADaM datasets; collaboration with biostatisticians and data managers is essential.
The position requires attention to data quality, reproducibility and documentation, with opportunities to contribute to study
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We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in…
United Kingdom
We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in…
Sale
Develop, maintain and validate SAS programs for clinical trial data. Create and validate analysis datasets, tables, listings and figures (TLFs).
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