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Senior Clinical Sas Programmer Jobs (NOW HIRING)

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

CICONIX, LLC

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Collabera

SAS Programmer

Jersey City, NJ · On-site

The role of the Senior Statistical Programmer is to perform statistical programming activities for ... This position performs statistical programming for clinical studies, integrated summaries, and in ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA · On-site

$145K - $156K/yr

Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and ... Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS)

SPECTRAFORCE

SAS Programmer

North Chicago, IL

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 ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

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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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Senior Clinical Sas Programmer jobs near you
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.

Senior Clinical Programmer - SDTM and R/SAS 3635027

Axiom Path

Bridgewater, NJ • Remote

$75 - $80/hr

Full-time

Posted 26 days ago

Job description

Be Part Of A High-Performing Team:

Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is bringing critical SDTM programming capabilities in-house and works closely with data management, biostatistics, and statistical programming. The environment is collaborative, technically rigorous, and well suited to an experienced programmer who enjoys building reliable clinical-data solutions while helping shape new internal processes.

What's In Store For You:

Engagement: W2 only (no C2C/1099)

This is a fully remote, 12-month consulting assignment open to candidates located anywhere in the United States. Availability during Eastern Time business hours is preferred.

The role offers the opportunity to become one of the early members of a growing clinical programming team and contribute directly to the organization’s transition from outsourced SDTM programming to an internal delivery model. A contract extension may be possible based on performance and business needs, although permanent conversion is not currently planned.

How You Will Make An Impact:

  • Create production-quality SDTM datasets using both SAS and R.
  • Independently perform quality control and validation of SDTM datasets.
  • Develop dataset specifications using CDISC standards and current SDTM Implementation Guides.
  • Create annotated CRFs, including domain mappings, annotation boxes, controlled terminology, and page-level placement.
  • Apply existing team macros and programming utilities to support annotated CRF and SDTM production.
  • Develop SAS- and R-based listings and reports supporting medical monitoring, clinical data management, and statistical endpoint monitoring.
  • Perform clinical-data checks, reconciliations, and issue investigation as assigned.
  • Collaborate closely with data managers, biostatisticians, statistical programmers, and clinical-study stakeholders.
  • Help establish scalable internal standards, workflows, and quality practices as SDTM programming transitions in-house.
  • Manage multiple study deliverables independently while maintaining accuracy, traceability, and timely execution.

Do you bring proven success in SDTM programming with both SAS and R?

  • Approximately 8–10 years of hands-on clinical programming experience in pharmaceutical, biotechnology, CRO, or related regulated clinical environments.
  • Strong production programming proficiency in both SAS and R.
  • Demonstrated experience creating and independently quality-checking SDTM datasets.
  • Strong knowledge of CDISC standards and current SDTM Implementation Guides.
  • Hands-on experience creating annotated CRFs, including page-level annotations and terminology mapping.
  • Ability to use established macros, functions, and programming utilities.
  • Experience translating raw clinical data, CRFs, specifications, and programming standards into compliant SDTM deliverables.
  • Strong analytical, troubleshooting, documentation, and quality-control skills.
  • Ability to work independently as an individual contributor in a small and evolving team.
  • Strong written and verbal communication skills.
  • Experience with JReview is highly preferred.
  • Experience with Shiny, Pharmaverse, or R Markdown is highly desirable.
  • Exposure to SQL programming is preferred.
  • Experience supporting medical monitoring, data-management reports, reconciliations, or statistical endpoint monitoring is beneficial.