- Base and Advance SAS® certified Programmer for SAS9 with more than 3 year of experience in clinical domain.
- Have a good knowledge of clinical trial process and I have experience in programming, analyzing, managing, transforming and reporting of clinical trials data using SAS environment.
- Understanding of the clinical trials Documents and Data (e.g. Study design and objectives, Baseline, Sample size, Randomization, Study populations, SDTM, safety and efficacy datasets).
- Works closely with the Biostatistics and Data Management member on various clinical projects and I have created DEMOGRAPHIC and ADVERSE EVENT safety tables.
- Comprehensively prepared reports using SAS repo..
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