and late phase clinical trials. Excellent skills in SAS programming and statistical reporting. Knowledge of CDISC standards...Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS...
Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming... Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document...
, Mathematics, Computer Science, or related applicable field. Minimum of 5 to 8 years' SAS programming experience in the... pharmaceutical/biotech industry with some experience using CDISC standards. Create source and validation programs using SAS software...
discipline. Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO... and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical...
most important research questions across clinical development, market access, and commercial use cases for our life sciences partners... with experience analyzing real-world data (e.g., healthcare claims or electronic health records) Excellent programmer in R (including...
, and statistical instructions. Develops and/or validates SAS programs to generate statistical output (e.g. TLFs) of clinical trial... Contract Research Organizations (CROs). Develops and tests SAS codes for clinical trial database logic checks. Assign tasks...