Clinical SAS Programmer

Abbott   •  

Saint Paul, MN

Industry: Healthcare

  •  

5 - 7 years

Posted 177 days ago

This job is no longer available.

JOB DESCRIPTION:

Primary Job Function

Responsible for building programs to create SAS datasets, tables, listings, and graphs from the clinical database while following the clinical study's protocol and statistical plans.

Core responsibilities

  • Build SAS datasets from clinical database.
  • Develop SAS macros, templates and utilities for data cleaning and reporting.
  • Utilize SDTM guidelines to build datasets.
  • 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.
  • 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.

Education/Experience Requirements:

BS/BA with 6+ years related work experience

* SAS Programming skills

* Clinical experience

* Knowledge of SDTM guidelines.

* Medical Device experiencepreferred.

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