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Senior Clinical Sas Programmer Jobs (NOW HIRING)

Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...

Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR); Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets ...

This position will have independence, but is expected to consult with either a senior individual ... focus SAS Skill Competencies: Accessing Data Creating Data Structures Managing Data Generating ...

We are seeking a highly skilled Senior SAS developer to support Clinical Data Automation with strong experience in SAS, R, and/or Python to support the development of automated clinical data ...

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer ... in clinical reporting and statistical programming * Strong competence in SAS/Base, SAS/Macro, and ...

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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 10, 2026, the average hourly pay for senior clinical sas programmer in the United States is $54.05, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $61.30 per hour, depending on experience, location, and employer.

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 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.
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Infographic showing various Senior Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,418 per year, or $54 per hour.

SAS Programmer

Spectra force

North Chicago, IL โ€ข On-site

Contractor

Re-posted 4 days ago


Job description

Company Description
SPECTRAFORCE TECHNOLOGIES INC (www.spectraforce.com) offers a powerful suite of IT and Consulting services allowing companies to embrace the challenges of meeting and exceeding the company's IT needs with an aggressive Total Cost of Ownership. We enable companies to focus on their core competencies, while we handle the integral details of building IT solution guaranteeing quality delivery with significant cost savings. We offer a competitive edge through our Staff Augmentation Services (PrimuSourcing) and Projects Outsourcing Services, which are powered by our Global Delivery Model with teams based onsite in the US and offshore in India.
Job Description
  • Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry.
  • Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of work experience on creating and validating ADaM datasets.
  • Experience with creating ADaM data specifications; such as ADSL, ADAE, BDS, controlled terminology, etc.
  • Experience on creating Tables, Listing and Figures for clinical study report using proc report or data _null_.
  • Knowledge of regulatory submission process, experience on creating ISS, ISE ADaM datasets and TLFs is a plus.
  • Efficient in using Excel and Word documents.
  • Excellent communication skill.
  • Experience in Immunology therapeutic area is preferred, A strong candidate, with experience in another TA, will certainly be considered.
  • Education - BS in Statistics, Computer Science or a related field with 6+ years of relevant experience OR MS in Statistics, Computer Science or a related field with 4+ years of relevant experience

Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.