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Clinical R Programmer Jobs in Chicago, IL (NOW HIRING)

... programmers develop intellectual property and assets to support the design and analysis of clinical ... Experience in SAS and/ or R statistical software packages. * Experience in study design and ...

... clinical, operational, and economic outcomes. You will influence technical strategy, drive ... Expertise in programming languages such as Python, R, SQL, SAS, or similar analytical tools.

... developers to translate research into clinically actionable insights for our clients. * Stay ... Demonstrated computational skills using R and SQL, specifically applied to large-scale healthcare ...

Data Scientist II, Outcomes Research

Chicago, IL ยท On-site +1

$100K - $150K/yr

... developers to translate research into clinically actionable insights for our clients. * Stay ... Demonstrated computational skills using R and SQL, specifically applied to large-scale healthcare ...

Scientist II, Translational Research

Chicago, IL ยท On-site +1

$100K - $150K/yr

Work with Product and Engineering teams to streamline workflow of computational analyze Contribute ... clinical and omics data. Proficient in R, Python, and SQ Previous experience working with large ...

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Clinical R Programmer information

See Chicago, IL salary details

$25

$66

$105

How much do clinical r programmer jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for clinical r programmer in Chicago, IL is $66.73, according to ZipRecruiter salary data. Most workers in this role earn between $55.24 and $75.53 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical R Programmer, and why are they important?

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are Clinical R Programmers?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What are some common challenges faced by Clinical R Programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Chicago, IL? For Clinical R Programmer jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Chicago, IL look for? The top searched job categories for Clinical R Programmer jobs in Chicago, IL are:
Infographic showing various Clinical R Programmer job openings in Chicago, IL as of July 2026, with employment types broken down into 85% Full Time, 5% Part Time, 5% Temporary, and 5% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $138,792 per year, or $66.7 per hour.
Study Design Statistician (US)

Study Design Statistician (US)

MMS

Chicago, IL โ€ข On-site

Full-time

Posted 8 days ago


Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?ย MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visitย www.mmsholdings.comย or follow MMS onย LinkedIn.
As part of ourย Strategic Statistical Servicesย Arm, this is a full-time role with emphasis on being an internalย and externalย SME for clinical trial design, together withย providing consultation to adviseย clients on a range of broader statistical issues, and will have an internal job title ofย Strategic Statistician.

Job Description:

Our experienced statisticians and programmers develop intellectual property and assets to support the design and analysis of clinical trials, precision medicine and real-world data analytics. We address the emerging analytics needs of the Industry with our biostatistics services, bespoke algorithms and unique, state of the art, proprietary, cloud-based trial simulation software KerusCloud. Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from:

  • Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives.
  • Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports.
  • Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality.
  • Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables.
  • Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity.
  • Support pre-sales discussions to understand and identify client needs, then contribute to technical solutions and resource/ cost estimates.
  • Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud.
  • Provide input and support to Marketing of KerusCloud, including demonstrations to clients, white papers, etc.

Requirements:

  • Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred.
  • 5-7 years of experience in the application of medical statistics (pharma, CRO, academic).
  • Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions.
  • Experience in delivering customer projects to high quality standards.
  • Experience in SAS and/ or R statistical software packages.
  • Experience in study design and protocol and report-writing preferred.
  • Experience of modelling and simulation techniques to explore complex study designs preferred.
  • Experience of Bayesian approaches to design and analysis of clinical data preferred.
  • Experience of early-phase drug development processes including innovative/ adaptive study design preferred.ย 

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M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980