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Senior Clinical Sas Programmer Jobs (NOW HIRING)

Tech Tammina LLC

Senior SAS Programmer

Okemos, MI · On-site

Senior SAS Programmer Location: Okemos, MI (Minimum 3 days onsite weekly) Duration: Long term Rate: Market f2f is must Responsibilities: · Participates in requirements and design sessions, then ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD · On-site

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 ...

University of Miami

SAS Programmer

Miami, FL · On-site

To learn how to apply for a faculty or staff position, please review this tip sheet. Sr. Research ... programmer to join an active clinical and translational research group focused on therapy ...

New

CICONIX, LLC

SAS Programmer

Fort Detrick, MD · On-site

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 ...

CICONIX, LLC

SAS Programmer

Frederick, MD · On-site

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 ...

University of Miami

SAS Programmer

Miami, FL · On-site

To learn how to apply for a faculty or staff position, please review this tip sheet. Sr. Research ... programmer to join an active clinical and translational research group focused on therapy ...

New

Tunnell Government Services

SAS Programmer

Bethesda, MD · On-site

Title: SAS Programmer Deliverables: * Prepare, update, and maintain all versions of statistical ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

SPECTRAFORCE

SAS Programmer

North Chicago, IL · On-site

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 ...

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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 Sep 12, 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 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.
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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 September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $112,418 per year, or $54 per hour.

Senior SAS/Statistical Programmer

Plainsboro, NJ • Remote

Wizsolution
51 - 200 employees
Learn more about Wizsolutionexternal

Full-time

Re-posted 3 days ago

Job description

Job Description

Company Descriptions:

Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our company is to connect high talent and motivated candidates to technical positions from our partner companies.

Job descriptions:

Senior SAS Programmer
Senior Statistical Programmer

*

-Perform SAS data manipulation and analysis programming
-May work with medical writing, clinical operations, and other clinical staff to support deliverables.
-Must work well both independently and with team members.
-Needs to be able to be on-time with deliverables, and for those deliverables to be of quality.
-Works with Statistician and Statistical programmer to assure results are consistent with expectations, and Quality control procedures are followed.
-Plans and carefully documents differences between programming results between program developer and Statistical QC programmer.
-Confirms that tracking sheets are current for projects, and may also confirm that results are consistent with earlier generated results.

·             MS with 3-5 +years of pharmaceutical industry experience.

·             Strong collaboration abilities and ability to work as part of a highly skilled team.

·             Experience in CDISC (SDTM, ADaM data sets)

·             Skilled in analysis of safety, efficacy & biomarker data, with an understanding of multiplicity issues; immunology/CV background a plus.

·             Experienced with standard and advanced statistical methods.

·             Expertise in SAS required, S-Plus or R preferred, including advanced statistical analysis, data integration, graphing & simulation.

·             Strong programming skills.

·             Good understanding of regulatory requirements & clinical trial design.

·             Knowledge of and ability to learn relevant clinical background and biomarker biology and incorporate these into statistical design, analysis & interpretation.

Preferred Qualifications:

Must have 3-5+ years SAS Programmer experience
SAS systems experience may include Base SAS, SAS/FSP,SAS SCL, Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system.

Job Type: Full-time