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Clinical R Programmer Jobs (NOW HIRING)

Parexel

Senior RWE Programmer

Fluency in SQL and R programming is required * Experience writing original code and performing raw data analysis (not derived solely from clinical trials) * Includes running analyses and/or ...

Parexel

Fluency in SQL and R programming isrequired * Experience writing original code and performing raw data analysis (not derived solely from clinical trials) * Includes running analyses and/or developing ...

GSK

Principal Statistical Programmer

Durham, NC · On-site

Expertise in R programming. * 6+ years of clinical programing experience * 5+ years of experience in the Pharmaceutical or Biotechnology industry. * Experience using generative AI tools and coding ...

Parexel

Fluency in SQL and R programming isrequired * Experience writing original code and performing raw data analysis (not derived solely from clinical trials) * Includes running analyses and/or developing ...

Parexel

Senior RWE/RWA Programmer

New Brunswick, NJ · On-site +1

Fluency in SQL and R programming isrequired * Experience writing original code and performing raw data analysis (not derived solely from clinical trials) * Includes running analyses and/or developing ...

Parexel

Senior RWE/RWA Programmer

Fluency in SQL and R programming is required * Experience writing original code and performing raw data analysis (not derived solely from clinical trials) * Includes running analyses and/or ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA

$145K - $156K/yr

Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS). * Comprehensive understanding of clinical trial processes, data flow, and clinical trial data ...

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Clinical R Programmer information

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How much do clinical r programmer jobs pay per hour?

As of Aug 6, 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 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 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 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:
Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Senior RWE Programmer

Parexel

Remote

Full-time

Posted 14 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

28th of 73 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel is seeking a Senior Real-World Evidence, RWE Programmer
Join a high-impact team as a remote Sr. Real-World Evidence Programmer,
supporting innovative work. You can work remotely out of Canada or the Continental United States.
If you are passionate about real-world data, advanced analytics,
and delivering meaningful insights, we encourage you to apply.
Who We Are Looking For
  • Effectively designs and codes R and SQL programs
    for assigned project(s), consistently meeting project objectives
  • Expert Coder: The ideal candidate spends most of their time hands-on coding versus project management or oversight responsibilities, has hands-on experience with raw RWE data including both claims data and Flatiron EHR and can write SQL code from scratch.
  • Advanced SQL Programming experience within the Real-World Data (RWD) domain is required.
  • Hands-on experience developing and managing data solutions in the Snowflake platform required.
  • Clean and validate Real-World Data (RWD)
  • to ensure consistency and reliability
  • Implement programming based on RWE protocols
    using a variety of RWD sources, including Optum and Flatiron
  • Leverage advanced statistical and epidemiological methodologies
    to deliver robust and reliable analyses
  • Create, review, and approve programming plans
    at both study and project levels
  • Demonstrate advanced knowledge
    of programming, epidemiological methodology implementation,
    and system development life cycle concepts
  • Maintain clear documentation
    of analytical programming and operational definitions
    to support reproducible and auditable RWE studies
  • Develop dashboards, reports, and presentations
    to effectively communicate findings
  • Collaborate with study team members
    to meet study timelines and recurring reporting deadlines

What You Will Do
  • Effectively designs and codes R and SQL programs for assigned project(s)
    consistently meeting objectives of the project.
  • Daily work % estimates: Coding (80%-90% of their daily work) + copying and pasting the numbers into the excel table shells (5%-20%)
  • Clean and validate RWD
    for consistency and reliability
  • Implement programming as specified from RWE protocol
    using a variety of RWD from multiple sources, including Optum and Flatiron
  • Leverage advanced statistical and epidemiological methodologies
    to deliver robust and reliable analyses
  • Create or review and approve programming plans
    at study and project level.
  • Displays highly advanced knowledge regarding program, epidemiology methodologies implementation
    and system development life cycle concepts.
  • Maintain clear documentation of analytical programming and operational definitions
    to support reproducible and auditable RWE studies
  • Develop dashboards, reports, and presentations
    to communicate findings
  • Work collaboratively with members of study teams
    to meet study and recurring report timelines

Who You Are
  • MS in data science, epidemiology, statistics, public health, or related discipline
  • At least 2-3 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations.
  • Hands-on experience with Flatiron data required; experience with Optum may be considered
  • Fluency in SQL and R programming is required
  • Experience writing original code and performing raw data analysis (not derived solely from clinical trials)
  • Includes running analyses and/or developing code for real-world analyses
  • Knowledge of SAS and/or Python is considered an advantage
  • Familiarity with US and global healthcare coding systems
    (e.g., ICD, CPT, HCPCS, LOINC, MedDRA)
  • And healthcare delivery systems (e.g., payers and reimbursement models)
  • Experience conducting routine and advanced statistical analyses for RWE generation
  • Including time-to-event, cross-sectional, and longitudinal data
  • Experience with big data analytical platforms
  • Deep understanding of observational study analysis
  • Ability to work independently and contribute to scrum development goals
  • In a fast-paced, flexible, team-oriented environment
  • Strong communication and collaboration skills
  • Competent in written and oral English.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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