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Clinical R Programmer Jobs in Princeton, NJ (NOW HIRING)

Parexel

Senior RWE/RWA Programmer

New Brunswick, NJ · Remote

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 ...

Amgen

Biostatistical Prograrmming Manager

New York, NY · On-site

... R programming for clinical trial analyses, data manipulation, reporting and visualization preferred Familiarity with additional programming languages and tools such as Python preferred Hands-on ...

NYULMC

Senior Bioinformatics Programmer

New York, NY · On-site

... in clinical care, biomedical research and medical education, is seeking highly motivated ... in Python, R, shell scripting • Proficiency in Nextflow, Django, Docker and Singularity ...

Pfizer

Manager, Clinical Pharmacology

New York, NY · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong ... Hands-on experience with common software tools for PK and PK/PD analyses (e.g., R, NONMEM, Monolix ...

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All JobsClinical R Programmer JobsClinical R Programmer Jobs in Princeton, NJ

Clinical R Programmer information

See Princeton, NJ salary details

$25

$67

$107

How much do clinical r programmer jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for clinical r programmer in Princeton, NJ is $67.90, according to ZipRecruiter salary data. Most workers in this role earn between $56.20 and $76.88 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 does a clinical programmer do?

A clinical programmer develops and maintains software for clinical trials, including programming data collection, validation, and analysis tools. They work with statistical teams to generate reports and ensure data accuracy, often using programming languages like SAS or R in a regulated environment.

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.

Is clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the healthcare and pharmaceutical industries, focusing on data analysis and reporting using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience. The role typically requires strong analytical skills and knowledge of clinical trial processes.

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 is the salary of a clinical data programmer?

The salary of a clinical data programmer typically ranges from $70,000 to $100,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with advanced skills in SAS, R, or SQL can earn higher salaries. Many roles also offer benefits such as health insurance and flexible schedules.

Which is better, CDM or SAS?

For a Clinical R Programmer, SAS is a widely used statistical software in clinical trials and regulatory submissions, offering robust data management and analysis capabilities. CDM (Clinical Data Management) refers to the process of handling clinical data, often using tools like SAS or dedicated CDM systems; the choice depends on project needs, but SAS proficiency is highly valued in the field.
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Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in Princeton, NJ as of June 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $141,234 per year, or $67.9 per hour.
Clinical Statistical Programmer

Clinical Statistical Programmer

Katalyst HealthCares & Life Sciences

Princeton, NJ • On-site

Other

Posted 28 days ago

Job description

Job Title

Responsibilities:

  • Generate and validate TLFs based on the Statistical Analysis Plan, TLF specifications, and industry best practices.
  • With minimal oversight, perform all programming activities and documentation for assigned studies.
  • Follow departmental Standard Operating Procedures (SOPs) and industry guidance to ensure traceability and regulatory compliance.
  • Support the preparation and review of the electronic regulatory submission.
  • Ensure that all deliverables are completed on time and of high quality.
  • Represent the Clinical Programming function at cross-functional meetings.
  • May support EDC development and visualization tools (PowerBI).

Requirements:

  • Minimum 3-5 years in a clinical programming role.
  • Bachelor's Degree (Data Science, Computer Science, Statistics, Bioinformatics, or related discipline).
  • Independently develop SAS/R programs to generate and validate datasets according to the Statistical Analysis Plan, TLF specifications, and industry best practices.
  • Experience generating outputs for regulatory submissions (FDA) MUST.
  • Programming experience in SQL, JSON (Good to have).
  • Working experience with relational databases. (EDC system, IBM (Zelta).
  • Experience implementing CDISC standards is desirable.
  • Knowledge of EDC development and visualization tools (PowerBI, Tableau) is an asset.
  • Excellent Communications skills, both oral and written.
  • Analytical skills, creativity and innovative approach to problem solving.
  • Propensity for continuous learning and experimentation.
  • Demonstrated initiative and problem-solving skills, critical thinking skills.
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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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