Program analysis programs and quality control checks of analysis data models, dataset specifications, statistical tables, figures, and listings for clinical trials; perform regulatory submission planning for FDAEMAPMDA or other agencies and support for regulatory questions; provide leadership at the project and therapeutic area levels on the design and implementation of standards that support statistical analysis and reporting, including integrated summary reports and summaries, and electronic submissions; perform statistical analysis using various SAS procedures such as Freq, Univariate, Means, Logistic, GLM, Mixed, and Lifetest procedures.

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