Description
Experience and Qualifications:-Strong SAS programming skills required, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL
-Experience in programming with clinical trial data and developing programs, testing, and documentation.
-Experience in handling SDTM mapping, related data structures, and programming to create SDTM data sets.
-Experience handling external data, e.g., laboratory data, PK, ECG, etc.
-Knowledge of developing reporting or other systems using SAS.
-Knowledge of data management process.
-Good understanding of data cleaning process.
-Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG.
-Good understanding of relational databases, e.g., ORACLE, and underlying data structure.
-Good understanding of system development life cycles, GCP, and related Regulatory guidelines.
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