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Independent Contractor Statistical Programmer Jobs in Chicago, IL

... independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS ... Good knowledge of statistical programming languages (including SAS). About InterSources Inc:

Senior SAS Programmer

Winnetka, IL · Remote

$87K - $111K/yr

Independently consult with committee members and CAP staff to define the focus, scope, and resources needed to complete each assigned statistical programming project. * Recommend, develop, and ...

Can review or develop ADAM specifications; can work with programmers and junior statisticians to ... Prepare and review statistical methods and results sections for the CSR independently in ...

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 ... Ability to work independently to efficiently accomplish specific responsibilities Infrastructure

Proficiency with SAS or R, and SQL, programming for data management and analysis * Commitment to ... Ability to work independently to efficiently accomplish specific responsibilities Infrastructure

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Independent Contractor Statistical Programmer information

See Chicago, IL salary details

$87K

$151.7K

$256.5K

How much do independent contractor statistical programmer jobs pay per year?

As of May 28, 2026, the average yearly pay for independent contractor statistical programmer in Chicago, IL is $151,732.00, according to ZipRecruiter salary data. Most workers in this role earn between $128,800.00 and $164,800.00 per year, depending on experience, location, and employer.
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Statistical Programmer

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Job description

Job Title

The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.

The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.

Develop and validate SAS programs to support clinical trial data analysis and reporting.

Create, maintain, and document SAS programming standards and procedures.

Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.

Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.

The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.

Prepare datasets for analysis, including merging and cleaning data from various sources.

Prepare and review tables, listings, and figures for clinical study reports.

Ensure compliance with regulatory requirements and guidelines.

Keep up to date with new SAS programming methods and software, as well as regulatory guidance.

Bachelor's Degree in statistics, computer science, or a similar quantitative field.

4+ years of clinical statistical programming experience within the pharmaceutical or related industry.

Proficiency in SAS programming.

Knowledge of CDISC data standards.

Strong attention to detail and ability to work independently.

Excellent problem-solving skills.

Excellent verbal and written communication skills.

Knowledge of regulatory requirements for clinical trials and drug development.

Ability to work in a team environment and collaborate effectively with other stakeholders.


Katalyst Healthcares & Life Sciences logo

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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