Veena Rao

Senior Clinical Sas Programmer @IQVIA India

Bengaluru, IN

The responsibilities involve the following:\\\\n Build SAS datasets from clinical database.\\\\n Develop SAS macros, templates and utilities for data cleaning and\\\\nreporting.\\\\n Utilize SDTM guidelines to build datasets.\\\\n Communicate with an internal team to create deliverables for\\\\npharmaceutical and biotechnology clients.\\\\n Implement analyses specified in the protocol or the Statistical Analysis\\\\nPlan (SAP) while working with the project statistician.\\\\n Ensure CRF meets the guidelines of the protocol and check for\\\\nconsistency and adequacy.\\\\n Write SAS programs to generate tables, listings, and figures and\\\\nanalysis datasets.\\\\n Review CRF annotations and data specifications.\\\\n Work in tandem with Biostatistics and Data Management member onvarious clinical projects.\\\\n Identify and edit checks per the data validation plan or data\\\\nmanagement plan.\\\\n Study management reports using SAS.\\\\n Validate the programmed analysis datasets, tables, listing and figures.\\\\n Perform analyses defined in the statistical analysis.\\\\n Prepare clinical and statistical summary reports.\\\\n Communicate with programming and statistics leads.\\\\n Utilize SAS programming skills within protocol team and perform all\\\\nprogramming required for clinical trial analysis and reporting.\\\\n Perform quality control on final reports.\\\\n Develop SAS coding and table templates for preparing, processing and\\\\nanalyzing clinical data.\\\\n Establish monitoring of data transfers for ongoing trials to identify study conduct or data issues\\\\n \\\\n\\\\n \\\\n \\\\n\\\\n \\\\n

International Institute of Information Technology Bangalore

Master of Data Science