SAS is widely used in clinical trial data analysis in pharmaceutical, biotech and clinical research companies. SAS programmers play an important role in clinical trial data analysis. In addition to doctors and clinicians who collect clinical trial data, the group conducting data analysis includes statisticians, clinical data managers(CDMs) and SAS programmers. Statisticians provide the ideas and methods of the data analysis, clinical data managers manage the collected data and control the data quality. In between, SAS programmers implement the analysis methods on the collected data and provide the study summary tables, data listing and graphs to the statisticians and or clinicians to write study report. SAS programmers work closely with statisticians and data managers.
Skills
- SAS Modules – SAS (Base, Macro, ODS, SQL, STAT, GRAPH, ACCESS)
- SAS Procedures – PROC MEANS, PROC SUMMARY, PROC UNIVARIATE, PROC TABULATE, PROC REG, PROC GPLOT, PROC LIFETEST
- Additional Software – MS Office Suite, MS Word, MS Excel, PowerPoint
- Operating Systems – UNIX, Windows
- Quality control associate – checks the accuracy of data entry and performs data audits
- Databases – Oracle Clinical
- Language – SQL, C, Java
- Other – ADaM, CDISC
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