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Sas Statistical Programmer Jobs (NOW HIRING)

InterSources

SAS / Statistical Programmer

Chicago, IL · On-site

Good knowledge of statistical programming languages (including SAS). About InterSources Inc: InterSources Inc, a Certified Diverse Supplier, was founded in 2007 and offers innovative solutions to ...

Xencor

CON-Statistical Programmer

San Diego, CA · On-site

$75 - $100/hr

More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... Strong experience with SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL in a Windows ...

Xencor

CON-Statistical Programmer

San Diego, CA · On-site

$75 - $100/hr

More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... Strong experience with SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL in a Windows ...

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How much do sas statistical programmer jobs pay per hour?

As of Jun 30, 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 June 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $119,333 per year, or $57.4 per hour.
SAS Statistical Programmer

SAS Statistical Programmer

Cardiovascular Research Foundation

Manhattan, NY • On-site

$85K - $95K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Key responsibilities

  • Develop and validate SAS programs for the analysis and reporting of clinical trial data.

  • Collaborate with biostatisticians and other clinical study team members to design and develop datasets, tables, figures, and listings for clinical study reports.

  • Oversee the development of programming documentation, including specifications and validation plans.

Job description

This role is subject to a flexible hybrid work arrangement requiring a minimum of 2 pre-determined days per week in our mid-town office.
SUMMARY
The SAS Statistical Programmer is responsible forproducing data analysis sets, listings, tables, ad hoc reports and validating programming as required for the effective operation and completion of clinical studies sponsored by CRF. The SAS Statistical Programmer is also responsible for the day-to-day development, maintenance and management of multiple clinical study databases and management of queries as requested by both internal and external sources.
ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Develop and validate SAS programs for the analysis and reporting of clinical trial data.
  • Ensure the accuracy and consistency of data outputs according to statistical analysis plans and specifications.
  • Collaborate with biostatisticians and other clinical study team members to design and develop datasets, tables, figures, and listings (TFLs) for clinical study reports.
  • Review and contribute to study documents, including protocols, statistical analysis plans, and case report forms.
  • Oversee the development of programming documentation, including specifications and validation plans.
  • Ensure compliance with industry standards and regulatory requirements, including CDISC standards and FDA guidelines.
  • Monitor and implement new technological tools and programming techniques to enhance the efficiency and quality of programming deliverables.
  • Participate in audits and inspections, addressing queries related to SAS programming.
QUALIFICATIONS
  • Bachelors' degree in Statistics, Biostatistics, Computer Science, or a related field.
  • Minimum of 1 year of SAS programming experience in a clinical trial environment within the pharmaceutical or biotechnology industry.
  • Strong knowledge of statistical methods and their application to the pharmaceutical industry.
  • Expertise in CDISC standards, including SDTM and ADaM.
  • Excellent problem-solving skills and the ability to work independently and collaboratively.
  • Strong communication and interpersonal skills, with the ability to explain complex technical concepts to non-technical stakeholders.
  • Proficient in the use of SAS software and familiarity with other statistical software packages.
BENEFITS
  • Choice of health plans include medical, Dental, and vision coverage
  • Company-paid short-term and long-term disability and life insurance
  • Health and dependent care flexible spending accounts
  • Pre-tax travel expenses through TransitChek program
  • 401(k) plan
  • Generous paid time off (PTO)
  • Fourteen paid holidays each year

COMPENSATION
The hiring range for this position is $85,000 - $95,000 per year. The annual salary that will ultimately be offered to the successful candidate will depend on job-related knowledge, education, skills, and experience.
CONTACT INFORMATION
To be considered for this opportunity, please submit your resume.
Be sure and visit our web site to learn more about how we strive to enhance and save patient lives every day www.crf.org
CRF is an equal opportunity employer.

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