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Senior Clinical Sas Programmer Jobs in Indiana (NOW HIRING)

Becton, Dickinson and Company

It takes the imagination and passion of all of us-from design and engineering to the manufacturing ... Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ...

Becton, Dickinson and Company

It takes the imagination and passion of all of us-from design and engineering to the manufacturing ... As a Manager, Clinical Applications , you will lead a team of Clinical Application Specialists ...

Ra

Marketing Analytics Manager

Indianapolis, IN · On-site

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in SAS or other statistical modeling tools. Who enjoys traveling, because this ...

Elevance Health

Data Scientist Senior

Indianapolis, IN · Hybrid

... of clinical programs. * Provide technical/analytical advice to staff. * Respond to and manage ad ... Three (3) years of experience with Python, R, SAS, or SAS Enterprise Miner; * Two (2) years of ...

Elevance Health

Data Scientist Senior

Indianapolis, IN · On-site

... of clinical programs. * Provide technical/analytical advice to staff. * Respond to and manage ad ... Three (3) years of experience with Python, R, SAS, or SAS Enterprise Miner; * Two (2) years of ...

Elevance Health

Data Scientist Senior

Indianapolis, IN · Hybrid

... of clinical programs. * Provide technical/analytical advice to staff. * Respond to and manage ad ... Three (3) years of experience with Python, R, SAS, or SAS Enterprise Miner; * Two (2) years of ...

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Senior Clinical Sas Programmer information

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How much do senior clinical sas programmer jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for senior clinical sas programmer in Indiana is $51.43, according to ZipRecruiter salary data. Most workers in this role earn between $38.41 and $58.32 per hour, depending on experience, location, and employer.

What is a senior clinical SAS programmer?

A Senior Clinical SAS Programmer is a specialized professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in pharmaceutical, biotechnology, or contract research organizations. They are responsible for developing, validating, and maintaining programs that transform raw clinical data into statistical tables, listings, and figures (TLFs) for regulatory submissions and study reports. In addition to technical programming tasks, senior SAS programmers often review code from junior programmers, ensure compliance with regulatory standards, and collaborate with statisticians, data managers, and clinical teams. Their expertise is critical for ensuring data integrity and supporting the success of clinical research projects.

What are the key skills and qualifications needed to thrive as a senior clinical SAS programmer?

To thrive as a Senior Clinical SAS Programmer, you need advanced proficiency in SAS programming, a solid understanding of clinical trial data, and typically a degree in statistics, computer science, or a related field. Expertise in CDISC standards (SDTM, ADaM), experience with clinical data management systems, and familiarity with regulatory submission requirements are essential technical qualifications. Strong analytical thinking, attention to detail, and effective communication skills help in collaborating with cross-functional teams and ensuring data quality. These skills ensure accurate data analysis, compliance with regulatory standards, and successful support of clinical research objectives.

What are some typical challenges faced by senior clinical SAS programmers when managing multiple clinical trial projects simultaneously?

Senior Clinical SAS Programmers often juggle multiple projects at various stages, which can present challenges such as prioritizing tasks, meeting tight regulatory deadlines, and ensuring data quality across studies. Effective communication and collaboration with statisticians, data managers, and clinical teams are essential to address emerging issues quickly. Familiarity with regulatory submission standards and proven organizational skills help in managing the workflow and maintaining consistency in deliverables.

What are the most commonly searched types of Clinical Sas Programmer jobs in Indiana?

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Senior Clinical Sas Programmer jobs near you

SR. CLINICAL SAS PROGRAMMER at cGxPServe Indianapolis, IN

Indianapolis, IN • On-site

Downtown Boulder Partnership
11 - 50 employees
Learn more about Downtown Boulder Partnershipexternal

$100 - $130/hr

Other

Posted 8 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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