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Sas Statistical Programmer Jobs (NOW HIRING)

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Performs quality control checks of SAS code and output produced by other Statistical Programmers to ensure accuracy and consistency within group * Demonstrates in-depth knowledge of clinical ...

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How much do sas statistical programmer jobs pay per hour?

As of Jul 1, 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.

How hard is it to get a job at SAS?

Securing a SAS Statistical Programmer position typically requires strong skills in SAS programming, data analysis, and understanding of clinical or research environments. Candidates with relevant certifications, such as the SAS Certified Data Scientist, and experience with data management and reporting tools often have better chances. Competition can vary based on location and experience level, but technical proficiency and industry knowledge are key factors.

How much do SAS Programmers make?

SAS Statistical Programmers typically earn between $70,000 and $120,000 annually, depending on experience, location, and industry. Senior roles or those with advanced skills in data analysis and clinical trial programming can earn higher salaries, especially with certifications and extensive experience.

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.

Are SAS Programmers in demand?

SAS Statistical Programmers are in demand in industries such as pharmaceuticals, healthcare, and clinical research due to their expertise in data analysis, programming, and regulatory compliance. The role often requires knowledge of SAS software, statistical methods, and sometimes certifications, with job growth driven by increasing data-driven decision-making in these sectors.

What is the average salary for a SAS programmer?

The average salary for a SAS statistical programmer typically ranges from $70,000 to $110,000 annually, depending on experience, location, and industry. Skilled programmers with certifications and knowledge of data analysis tools may earn higher salaries.

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.
Lead Statistical Programmer

Lead Statistical Programmer

Katalyst HealthCares & Life Sciences

Tarrytown, NY • On-site

Other

Posted 14 days ago

Key responsibilities

  • Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.

  • Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.

  • Provide leadership and project management for programming tasks supporting clinical trial activities.

Job description

Job Title

Responsibilities:

  • Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
  • Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
  • Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, and other clinical publications; support systems to produce electronic regulatory submissions.
  • Assist in establishing standardized programming procedures and work instructions.
  • Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
  • Develop and maintain clinical processing workflow systems.
  • Assist in the development of client proposal documents.
  • Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
  • Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
  • Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
  • Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
  • Assist in updating/writing PROMETRIKA standard operating procedures (SOPs).
  • Develop tools in SAS® for data analysis and reporting that comply with regulatory requirements.
  • Develop specifications (e.g., metadata files), annotate CRFs and create SAS® programs for the mapping of raw datasets to CDISC SDTM standards.
  • Create define.xml files from metadata files for SDTM and ADaM.
  • Convert data received in other formats to SAS® datasets.

Requirements:

  • Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
  • Knowledge of SDTM, ADaM, FDA and ICH guidance.
  • Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
  • Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
  • Consistent experience as a lead statistical programmer on several concurrent projects.
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
  • Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
  • Excellent analytical skills.
  • Proven ability to learn new systems and function in an evolving technical environment.
  • Ability to negotiate and influence to achieve results.
  • Good presentation skills.
  • Good business awareness/business development skills (including financial awareness).
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Knowledge of other programming languages and database management software packages is a plus.
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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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