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Senior Statistical Programmer Jobs in Illinois (NOW HIRING)

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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 ...

Zoro

Senior Analyst, Marketing Science

Chicago, IL

$105.60K - $130.30K/yr

The Senior Analyst, Marketing Science will use customer and marketing data to generate actionable ... Expert proficiency in SQL and statistical programming languages (R or Python) for data manipulation ...

Agoda

Senior Product Manager (Japan)

Chicago, IL · On-site

$130.40K - $172.20K/yr

They are seeking a Senior Product Manager who will drive product strategy and collaborate with ... Computer Science, Statistics, Engineering, Mathematics, or similar quantitative discipline) • ...

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How much do senior statistical programmer jobs pay per year?

As of May 28, 2026, the average yearly pay for senior statistical programmer 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 is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.
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Senior Statistical Programmer jobs near you
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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