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Clinical R Programmer Jobs (NOW HIRING)

Our programmers work directly with Clinical Operation teams to identify needs and establish ... Contribute to internal R package development for efficient cross-departmental programming practices;

Our programmers work directly with Clinical Operation teams to identify needs and establish ... Contribute to internal R package development for efficient cross-departmental programming practices;

Our programmers work directly with Clinical Operation teams to identify needs and establish ... Contribute to internal R package development for efficient cross-departmental programming practices;

Our programmers work directly with Clinical Operation teams to identify needs and establish ... Contribute to internal R package development for efficient cross-departmental programming practices;

R Programmer

Cincinnati, OH · On-site

$85 - $120/hr

Our programmers work directly with Clinical Operation teams to identify needs and establish ... Contribute to internal R package development for efficient cross-departmental programming practices;

Using expertise in R programming and clinical trials to create solutions that will enable an open-source ecosystem for programming. This role will coordinate gathering and prioritizing requirements ...

This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...

This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes ... Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ...

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Clinical R Programmer information

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$24

$64

$102

How much do clinical r programmer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical r programmer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What is a Clinical R programmer?

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 skills and qualifications are needed to be a Clinical R programmer?

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 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.

More about Clinical R Programmer jobs

What cities are hiring for Clinical R Programmer jobs?

Cities with the most Clinical R Programmer job openings:

What states have the most Clinical R Programmer jobs?

States with the most job openings for Clinical R Programmer jobs include:

What job categories do people searching Clinical R Programmer jobs look for?

The top searched job categories for Clinical R Programmer jobs are:

Infographic showing various Clinical R Programmer job openings in the United States as of August 2026, with employment types broken down into 79% Full Time, 5% Part Time, and 16% Contract. Highlights an 84% In-person, 5% Hybrid, and 11% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

R Programmer

Cincinnati, OH • On-site


Medpace, Inc.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 74 rated research

Great coworkers

People enjoy working here

Good employer


Other

Medical, Retirement, PTO

Posted 22 days ago


Job description

Job Summary
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our programmers work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Programmers will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Programmers will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering teams.
Responsibilities
  • Evaluate data needs for assigned projects and make recommendations on strategic approach specific to the study design;
  • Work alongside operational and medical leads to contribute innovative data products (primarily Shiny applications);
  • Contribute to internal R package development for efficient cross-departmental programming practices;
  • Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting;
  • Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and
  • Support departmental process improvement initiatives.

Qualifications
  • Bachelor's in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field;
  • Analytical thinker with great attention to detail;
  • Ability to prioritize multiple projects on a sprint schedule;
  • Excellent verbal communication skills;
  • Programming experience in R;
  • Work experience with clinical data;
  • Experience building web applications is preferred (with either Shiny or Streamlit); and
  • Experience building dashboards is preferred (with either PowerBI, Tableau, or Spotfire).

Additional Considerations
We are hiring all levels of experience. Degree level, work experience, interview performance, and programming proficiency will be considered. Prior to the interview stage, a programming assessment will be conducted, details will be shared with candidates during scheduling confirmation.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992


What Medpace employees say

Pay

Benefits

Hours and flexibility

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