to early and late phase clinical trials. Excellent skills in SAS programming and statistical reporting. Knowledge of CDISC...Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS...
-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results... of SDTM and ADAM specifications for assigned studies. Requirements: Thorough understanding of clinical trial reporting...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment... and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical...
is preferred (statistics, biostatistics, or closely related field). 5 years' experience with SAS and clinical programming...Responsibilities: Lead the development, validation, and maintenance of statistical programs using SAS to generate...
for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings..., and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret study...