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Associate Sas Programmer Jobs in Oak Brook, IL (NOW HIRING)

... engineering, environmental science or a related field. A GPA of 3.5 or higher is highly desirable ... Proficiency in Excel is required; experience with MS SQL Server, R, Python, Stata, SAS, Tableau ...

2027 Summer Associate (Intern)

Chicago, IL

$15.50 - $20.50/hr

... Stata,SAS,Python, or Snowflake. * Interact with senior staff,experts,and clients ... Experience with statistical, econometric and programming tools such as Excel, Stata, R, Python ...

Accounting, Engineering, Data Processing/Analytics/Science, Computer and Information Science ... SAS) - Utilizing advanced data analysis techniques to drive insights - Developing complex data ...

New

Manipulate data in a SAS, SQL, and Hadoop environment to create actionable insights aligned to ... or engineering. * CDW Summer Internship experience * Proficient with Microsoft Office, including ...

New

Manipulate data in a SAS, SQL, and Hadoop environment to create actionable insights aligned to ... or engineering. * CDW Summer Internship experience * Proficient with Microsoft Office, including ...

New

Manipulate data in a SAS, SQL, and Hadoop environment to create actionable insights aligned to ... or engineering. * CDW Summer Internship experience * Proficient with Microsoft Office, including ...

New

Software Engineer

Chicago, IL · On-site

$61K - $121K/yr

Provide constructive peer feedback and begin mentoring associate-level engineers. Qualifications ... Exposure to machine learning, natural language processing, Python, R, or SAS preferred. * You must ...

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Associate Sas Programmer information

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$80

How much do associate sas programmer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for associate sas programmer in Oak Brook, IL is $49.46, according to ZipRecruiter salary data. Most workers in this role earn between $34.71 and $62.12 per hour, depending on experience, location, and employer.

What is an Associate SAS Programmer?

An Associate SAS Programmer is an entry-level professional who specializes in using SAS (Statistical Analysis System) software to manage, analyze, and report data. They typically assist more senior programmers and statisticians in preparing datasets, writing code, and generating statistical reports, often within industries such as healthcare, finance, or research. This role requires a good understanding of SAS programming language, attention to detail, and the ability to follow standard operating procedures. Associate SAS Programmers often work as part of a larger data or analytics team, supporting projects by ensuring data integrity and accurate analyses.

What are the typical responsibilities of an Associate SAS Programmer?

As an Associate SAS Programmer in clinical research, you will primarily be responsible for writing and validating SAS programs to analyze clinical trial data, generate tables, listings, and figures, and ensure data integrity and compliance with regulatory standards. Your daily tasks may also include collaborating closely with statisticians, data managers, and senior programmers to review requirements and resolve data issues. This role often involves learning industry best practices and becoming familiar with CDISC standards, offering a strong foundation for career advancement in clinical data programming.

What are the key skills and qualifications needed to thrive as an Associate SAS Programmer?

To thrive as an Associate SAS Programmer, you need a solid understanding of statistical analysis, data management, and proficiency in SAS programming, often supported by a degree in statistics, computer science, or a related field. Familiarity with SAS software, data visualization tools, and knowledge of regulatory requirements or CDISC standards are typically expected, and SAS certification can be an advantage. Attention to detail, problem-solving ability, and effective communication are key soft skills for this role. These skills are crucial for ensuring accurate data analysis, efficient workflow, and clear reporting in data-driven environments such as clinical research or business analytics.

What are the most commonly searched types of Sas Programmer jobs in Oak Brook, IL?

The most popular types of Sas Programmer jobs in Oak Brook, IL are:

What cities near Oak Brook, IL are hiring for Associate Sas Programmer jobs?

Cities near Oak Brook, IL with the most Associate Sas Programmer job openings:

Infographic showing various Associate Sas Programmer job openings in Oak Brook, IL as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,870 per year, or $49.5 per hour.

Associate Director of Biostatistics (Remote)

Astrix Inc

Lombard, IL • On-site, Remote

$170K - $215K/yr

Full-time

Re-posted 12 days ago


Job description

Pay Rate Low: 170000 | Pay Rate High: 210000
Our client is a growing contract research organization seeking an Associate Director, Biostatistics to provide scientific leadership and people management across multiple clinical studies! They focus on collaborative, growth oriented culture & offers competitive compensation and benefits!
Title: Associate Director, Biostatistics (Remote)
Location: Remote - United States
Salary: $170k - $215k+(Depends on experience)
Position Overview
Excellent leadership role supporting impactful clinical research programs! This fully remote role serves as a first-line manager with accountability for statistical quality, project execution, and team development in support of clinical development programs.
Key Responsibilities
  • Lead and manage a team of statisticians, ensuring high-quality statistical deliverables and on-time study execution
  • Oversee statistical resourcing across multiple clinical trials
  • Provide strategic and scientific input to clinical development programs
  • Author, review, and approve protocols, Statistical Analysis Plans (SAPs), and table shells
  • Collaborate cross-functionally with Programming, Data Management, and Clinical Operations
  • Contribute to clinical study reports, regulatory submissions, and data presentations

Qualifications
  • MS in Biostatistics, Statistics, Mathematics, or related field
  • Minimum 7 years of clinical trials experience with a Master's degree, or 5 years with a PhD
  • Strong proficiency in SAS and/or R
  • Solid understanding of statistical methods used in pharmaceutical and clinical research
  • Excellent communication and stakeholder-facing skills
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