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Senior Statistical Programmer Analyst Jobs in Illinois

NorthShore PC Service

Programmer Analyst III

Skokie, IL · On-site

$52.24 - $80.97/hr

As the Programmer Analyst III at Endeavor Health, you will be the expert resource responsible for ... Serve as the most senior technical resource on the team and provide support for the manager in ...

NorthShore

Programmer Analyst III

Skokie, IL · On-site

$52.24 - $80.97/hr

As the Programmer Analyst III at Endeavor Health, you will be the expert resource responsible for ... Serve as the most senior technical resource on the team and provide support for the manager in ...

cap

Senior SAS Programmer

Winnetka, IL · Remote

$87K - $111K/yr

Brief Description The Senior SAS Programmer in the Biostatistics Department is responsible for ... Having the experience and expertise to handle complex research or development statistical ...

Northwestern University

Statistical Analyst

Evanston, IL · On-site

$70.02K - $80K/yr

Proficiency with SAS or R, and SQL, programming for data management and analysis * Commitment to ... senior/adult care. Visit us at to learn more. Professional Growth & Development: Northwestern ...

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How much do senior statistical programmer analyst jobs pay per year?

As of May 28, 2026, the average yearly pay for senior statistical programmer analyst in Illinois is $124,320.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,700.00 and $143,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Statistical Programmer Analyst, and why are they important?

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.

How does a Senior Statistical Programmer Analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.

What does a Senior Statistical Programmer Analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.
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Senior Statistical Programmer

Senior Statistical Programmer

Katalyst HealthCares & Life Sciences

Antioch, IL • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Senior Statistical Programmer

We are seeking a highly motivated and qualified individual to join our Clinical Department as a Senior Statistical Programmer and work as part of a team to drive success.

Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team.

The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses.

This position requires close collaboration with cross-functional teams to ensure the integrity and accuracy of clinical data used in regulatory filings and internal reporting.

Responsibilities:
  • Independently develop, validate, document and troubleshoot SAS programs for the preparation of periodic internal reports, regulatory submissions, and ad hoc analyses.
  • Create and maintain analysis and submission datasets (ADaM, SDTM) in compliance with CDISC standards and regulatory guidance.
  • Design, develop, validate, update, and document SAS programs to generate analysis datasets, data listings, tables, and graphs of high quality in a timely manner.
  • Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies.
  • Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
  • Develop software tools, SAS macros and utilities to automate programming activities and improve programming efficiency and quality.
  • Create SAS macros or other tools to enhance the efficient delivery of statistical services, providing associated documentation and staff training as needed.
  • Program quality checks for clinical study raw data and report findings.
  • Review or author SDTM and ADaM specifications and datasets.
  • Manage CROs, including reviewing or validating statistical deliverables of vendors.
  • Provides input in the design and development of case report forms.
  • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience.
  • Establish and maintain excellent working relationships with critical collaborative partners throughout the company.
Requirements:
  • Bachelor's degree in Biostatistics, Mathematics, Statistics, Computer Science, or related field
  • Minimum 6 years' experience in bio-pharma statistical programming
  • Advanced SAS programming skills in SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL with a demonstrated mastery of SAS/STAT procedures
  • Strong expertise in CDISC including SDTM, ADaM, and CDASH
  • Extensive experience in SAS macro functions and dynamic code generations.
  • Experience in regulatory submissions (e.g., NDAs and DSURs)
  • High attention to detail, with a focus on quality and traceability in all deliverables
  • Strong interpersonal and teamwork skills with a collaborative mindset and the ability to manage multiple priorities in a fast-paced and dynamic environment with shifting timelines and evolving needs
  • Take initiatives to solve problems proactively and think critically
  • Willing to adapt to changing business needs, able to pivot between tasks
  • Able to make complex programming and data-related decisions independently
  • Comprehensive knowledge and deep understanding of statistical programming environments, processes, procedures, and roles for clinical development from Phase 1 through regulatory submission
  • Up to date with CDISC standards, industry trends, best practices, and statistical programming methodology.
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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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