•SAS Programmer with about 4 years of experience in clinical domain.
•Exposure of working on Phase I-III Clinical Trials.
•Knowledge of Base SAS, SAS macros, SAS/SQL, SAS/ODS, SAS/GRAPH, SAS STAT etc procedures.
•Experienced in using SAS Procedures, SAS functions, dataset options & advanced macro programming.
•Created SDTM Datasets in compliance with CDISC standards.
•Annotated CRF based on CDISC compliance.
•Extensive experience of creating Table, Listing, Figures, Analysis Datasets.
•Experience of define.xml.
•Experience in creating test scenarios to find errors and confirm programs meet specifications.
•Develop SAS macros for general use and to reduce programming effort.
•Proactive and highly motivated towards the job. Ability to adapt to different working environment.