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Sas Statistical Programmer Jobs (NOW HIRING)

Systimmune

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

Develop SAS programs and macros to automate dataset generation and reporting deliverables. * Contribute to process improvements and enhancements of the statistical programming environment.

MSD

Senior Statistical Programmer

Rahway, NJ

Significant SAS or R programming experience for data manipulation, analysis and reporting * Designs ... Implements statistical methods not currently available through commercial software packages

LivaNova

Statistical Programmer II

Hapeville, GA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Austin, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Dallas, TX · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Boston, MA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Phoenix, AZ · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Atlanta, GA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Houston, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Minneapolis, MN

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

MSD

Senior Statistical Programmer

North Wales, PA

Significant SAS or R programming experience for data manipulation, analysis and reporting * Designs ... Implements statistical methods not currently available through commercial software packages

LivaNova

Statistical Programmer II

Atlanta, GA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Raleigh, NC · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

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SAS Statistical Programmer information

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How much do sas statistical programmer jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for sas statistical programmer in the United States is $57.37, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $85.34 per hour, depending on experience, location, and employer.

What types of projects do Sas Statistical Programmers typically work on, and how do they collaborate with other teams?

Sas Statistical Programmers often work on projects involving the analysis and reporting of clinical trial or observational study data, producing datasets, tables, listings, and figures to support regulatory submissions or scientific publications. They routinely collaborate with biostatisticians, clinical data managers, and project managers to ensure data quality and compliance with industry standards. Daily responsibilities include coding in SAS, validating datasets, troubleshooting data issues, and preparing documentation. Effective communication and teamwork are essential, as the role frequently involves working in multidisciplinary teams to meet project goals and timelines.

What is a SAS Statistical Programmer job?

A SAS Statistical Programmer is a professional who utilizes SAS software to manage, analyze, and report statistical data, primarily in industries like pharmaceuticals, healthcare, and clinical research. They write and validate programs to generate tables, listings, and figures for clinical trials or other data-driven studies. Their role involves ensuring data accuracy, compliance with regulatory guidelines, and collaboration with statisticians and researchers to support decision-making.

What are the key skills and qualifications needed to thrive in the Sas Statistical Programmer position, and why are they important?

To thrive as a Sas Statistical Programmer, you need a strong background in statistics, programming (especially SAS), and data management, usually supported by a degree in statistics, computer science, or a related field. Familiarity with SAS Base, SAS Macro, and clinical data standards like CDISC, as well as relevant industry certifications, are commonly required. Attention to detail, strong problem-solving abilities, and effective communication skills are valuable soft skills. These competencies ensure accurate data analysis, clear reporting, and successful collaboration within cross-functional teams in fields like healthcare or pharmaceuticals.

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SAS Statistical Programmer jobs near you
Infographic showing various Sas Statistical Programmer job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 7% Part Time, 1% Temporary, 6% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $119,333 per year, or $57.4 per hour.
Statistical Programmer

Statistical Programmer

Systimmune

Redmond, WA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The Statistical Programmer will support statistical programming activities for clinical trials, including generating SDTM/ADaM datasets, tables, figures, and listings (TFLs). This role is ideal for someone early in their career who is eager to learn and grow in a fast-paced biotech environment with exposure to end-to-end clinical development.
This position is full-time onsite at our Redmond, WA location and we will be moving to our new location in Bothell, WA fall 2026. We will consider candidates for our Princeton, NJ location on a case by case basis. 
Responsibilities
  • Collaborate with biostatisticians and cross-functional study team members to deliver statistical analysis and reporting outputs in line with project timelines.
  • Review study documents including statistical analysis plans (SAPs), CRFs, database specifications, and data transfer specifications.
  • Create and/or review SDTM/ADaM mapping specifications and annotated CRFs (aCRFs).
  • Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer’s guides.
  • Develop and validate tables, figures, and listings (TFLs) to support clinical study analyses, regulatory submissions, conferences, and publications.
  • Assess the quality, integrity, and consistency of analysis datasets, including cross-study analyses where applicable.
  • Develop SAS programs and macros to automate dataset generation and reporting deliverables.
  • Contribute to process improvements and enhancements of the statistical programming environment.
  • Participate in study team meetings and representing statistical programming in cross-functional discussions.
  • Apply knowledge of clinical trial design, CDISC standards, and regulatory requirements while producing analysis datasets and outputs in compliance with SOPs and industry standards.
 
Qualifications
  • Master’s degree or higher in Biostatistics, Statistics, Mathematics, or a related scientific discipline, with 0–2 years of experience in statistical programming within the pharmaceutical/biotech industry or a CRO.
  • Proficiency in SAS programming, preferably with experience in a clinical trial environment.
  • Working knowledge of CDISC standards (SDTM and ADaM).
  • Hands-on experience in developing and validating SDTM and ADaM datasets, as well as statistical outputs (tables, figures, and listings).
  • Prior experience or exposure to oncology studies is preferred.
  • Strong analytical, problem-solving, and organizational skills.
  • Effective communication and interpersonal skills, with the ability to work collaboratively in cross-functional teams.

Compensation and Benefits:
The expected base salary range for this position is $80,000 - $100,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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