Clinical SAS Programmer

Overview

On Site
Full Time

Skills

Data Manipulation
Reporting
Clinical Trials
Statistics
Mathematics
Computer Science
Pharmaceutics
CDISC
SAS
SDTM
Macros
SAS/GRAPH
Microsoft Word
Microsoft Excel
Microsoft PowerPoint

Job Details

Responsibilities:
  • Perform data manipulation, analysis and reporting of primarily clinical trial data.
  • Create SDTM data sets.
  • Create analysis data sets.
  • Program and generate tables, listings and graphs (TLGs).
  • Validate and document SAS programs and output.
  • Fulfil ad-hoc analysis requests.
  • Other services as needed.
Requirements:
  • Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field.
  • Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards.
  • Create source and validation programs using SAS software for SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products.
  • Integrates data across multiple studies or drug programs.
  • Expertise in the development and use of system-level macro programs.
  • Experience in programming using SAS/GRAPH.
  • Proficient in Microsoft Word, Excel, and PowerPoint.
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