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.

• Build SAS datasets from clinical database.

• 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.

• 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​.