SR. CLINICAL SAS PROGRAMMER at cGxPServe Indianapolis, IN

Downtown Boulder Partnership; Indianapolis (IN); On-site; USD 100,000 - 130,000; Full time

Job summary

Downtown Boulder Partnership is seeking an experienced SAS Programmer in Indianapolis, Indiana. The ideal candidate will have a minimum of ten years of SAS programming experience in the pharmaceutical or biotech industry, with a strong understanding of CDISC standards and a background in scientific disciplines.

The role involves critical responsibilities such as data manipulation, analysis, and generating comprehensive reports of clinical trial data. Proficiency in using SAS software is essential for creating various datasets and tables.

Qualifications

• Bachelor's degree or higher, preferably in a scientific discipline.
• Minimum of 10 years' SAS programming experience in the pharmaceutical/biotech industry.
• Ability to create source and validation programs using SAS.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Develop and maintain department/system-level macros.
• Program and generate tables, figures, and listings (TFLs).

Skills

SAS programming

Data analysis

CDISC standards

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Education

Bachelor's degree in Statistics, Mathematics, or Computer Science

Tools

SAS Software

SAS/GTL

Job description

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Develop and maintain department/system-level macros.
• Create and review SDTM and Adam specifications.
• Create and validate SDTM data sets.
• Create and validate analysis data sets.
• Create and validate patient profiles.
• Program and generate tables, figures, and listings (TFLs).
• Validate and document SAS programs and outputs.
• Fulfil ad-hoc analysis requests.
• Provide other services.

Requirements

• Bachelor's degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or a related applicable field.
• Minimum of ten (10) years' SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
• Ability to create source and validation programs using SAS software for SDTM datasets, Adam datasets, and tables, figures, and listings (TFLs) for multiple studies/products.
• Experience integrating data across multiple studies or drug programs.
• Expertise in developing and using system-level macro programs.
• Experience programming with SAS/GTL.
• Proficiency in Microsoft Word, Excel, and PowerPoint.