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How Does Clinical SAS Programmer Work

Step By Step SAS Training offers a comprehensive course on CDISC (Clinical Data Interchange Standards Consortium), essential for professionals in the pharmaceutical and clinical research sectors. Participants delve into the fundamentals of CDISC standards, learning to implement them effectively in clinical trials and regulatory submissions. Through practical examples and hands-on exercises, learners gain proficiency in converting raw clinical data into CDISC-compliant datasets, ensuring interoperability and regulatory compliance.

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How Does Clinical SAS Programmer Work

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  1. How Does Clinical SAS Programmer Work

  2. Clinical SAS Programmer works on clinical data for a variety of pharmaceutical and biotechnologyclients. The Clinical SAS Programmers build the appropriate programs using Base and Advanced SASconcepts to create SASdatasets from the clinical database, external data sources and other data sources as outlined inthe clinical study's protocol or statistical plans or mock shells. The Clinical SAS Programmer will develop SASmacros, templates and utilities for data cleaning and reporting. The Clinical SAS Programmerhas working knowledge of SDTM and ADaMGuidelines. Review CRF’s to ensure consistency with protocol and adequacy to collect the data to meetthe objectives defined in the statistical section of the protocol.Review CRF annotations and database data specifications. Creates derived-analysis datasets. Executes analyses specified in the protocol or theStatistical Analysis Plan (SAP) under the guidance of the project statistician. Works closely with the Biostatistics and Data Management member on various clinicalprojects.Interface with data management and clinical to identify and program edit checks per theData Validation Plan/Data Management Plan and study management reports using SAS.Write SAS programs to generate tables, listings, and figures and analysis datasets.Perform validation of the programmed analysis datasets, tables, listing and figures.Perform analyses defined in the statistical analysis plan as well as adhoc analyses as requested. Participate in the preparation of clinical and statistical summary reports.

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