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Sas Programmer Clinical Data Validation Macro Jobs

Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Experience clarifying business and technical requirements with data requestors * Provides technical ... Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.

... Programmer) to support SAS modernization efforts by analyzing existing workflows and developing ... and validate SAS conversion complexity and feasibility • Develop and optimize data pipelines ...

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Sas Programmer Clinical Data Validation Macro information

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How much do sas programmer clinical data validation macro jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for sas programmer clinical data validation macro in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

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Infographic showing various Sas Programmer Clinical Data Validation Macro job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

SR. CLINICAL SAS PROGRAMMER at cGxPServe Indianapolis, IN

Indianapolis, IN • On-site

Downtown Boulder Partnership
11 - 50 employees

Other

Posted 22 days ago


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.
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