Clinical SAS Programming

• Responsible for building programs to create SAS datasets from the clinical database, external data sources, and other sources while following the clinical study's protocol or statistical plans.

Primary Responsibilities:

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

Other Details:

• Free Clinical SAS Programming Practical Training and Placement
• Benefits: Dummy Project, Every Day Assignment, Resume preparation