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Clinical R Programmer Jobs in Apex, NC (NOW HIRING)

Demonstrated programming skills in R (required), including experience developing reproducible ... Knowledge of Good Clinical Practice (GCP), quality assurance principles, and regulatory ...

Demonstrated programming skills in R (required), including experience developing reproducible ... Knowledge of Good Clinical Practice (GCP), quality assurance principles, and regulatory ...

Work with large healthcare datasets to generate insights that support regulatory, clinical, and ... Proficiency in statistical programming (e.g., R, SAS, or Python) and experience working with health ...

Work with large healthcare datasets to generate insights that support regulatory, clinical, and ... Proficiency in statistical programming (e.g., R, SAS, or Python) and experience working with health ...

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Clinical R Programmer information

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How much do clinical r programmer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for clinical r programmer in Apex, NC is $49.36, according to ZipRecruiter salary data. Most workers in this role earn between $40.87 and $55.87 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 Apex, NC? For Clinical R Programmer jobs in Apex, NC, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Apex, NC look for? The top searched job categories for Clinical R Programmer jobs in Apex, NC are:
What cities near Apex, NC are hiring for Clinical R Programmer jobs? Cities near Apex, NC with the most Clinical R Programmer job openings:
Senior Biostatistician

Senior Biostatistician

RTI International

Raleigh, NC โ€ข On-site, Remote

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 26 days ago


Job description

About the Hiring Group

RTI Health Solutions (RTI-HS), a wholly owned subsidiary of RTI International, is an independent and internationally recognized research organization.ย With offices inย the US, UK, Spain, France, and Sweden, we provide healthcare consulting and research expertise to optimize decision making for pharmaceutical, biotechnology, and medical device products across the development and marketing lifecycle. Clients rely on our expertise, quality standards, and integrity to guide their product development and regulatory and market access strategies. Our various practice areas include Value, Access, and HEOR; Patient-Centered and Outcomes Research; Epidemiology and Biostatistics; Medical Communications; Global Business Operations; and Strategic Consulting and Growth.

We are currently seeking a Senior Biostatistician to join our growing Biostatistics team. In this role, you will perform statistical research tasks of moderate to high technical complexity, with a strong focus on causal inference methods and target trial emulation using real-world data. You will contribute to the development of statistical analysis plans, conduct analyses, and support proposal development under limited supervision while collaborating closely with multidisciplinary project teams on regulatory-grade research deliverables.

This role may be hybrid or fully remote, with a strong preference for candidates located in North Carolina.

As part of the application process, candidates are required to submit a short cover letter outlining their relevant experience and alignment with the role.

What You'll Do
  • Plan, conduct, and document statistical analyses for observational studies and clinical trials, with an emphasis on causal inference methods.
  • Implement target trial emulation analyses using real-world data sources.
  • Develop simple to moderately complex statistical analysis plans and contribute to more complex SAPs under supervision.
  • Write statistical sections of study reports, protocols, and proposals.
  • Ensure the quality, accuracy, and timeliness of statistical analyses and programming outputs.
  • Provide statistical and methodological solutions to internal, cross-functional project teams.
  • Mentor and oversee less experienced staff on selected project tasks.
  • Learn and apply new statistical methods in response to evolving project and research needs.
  • Contribute to the scientific reputation and professional development of the biostatistics group and prepare presentations for external audiences.

To be successful in this role, you will have strong analytical, organizational, and problem-solving skills; a high level of written and verbal communication skills, and the ability to manage multiple tasks, meet timelines, and work effectively in collaborative team environments.

What You'll Need
  • Master's degree and 6 years of experience, PhD and 1 years of experience, or equivalent combination of education and experience.
  • Demonstrated programming skills in R (required), including experience developing reproducible analysis pipelines.
  • Demonstrated experience with causal inference methods (e.g., propensity score methods, weighting, marginal structural models)
  • Demonstrated experience analyzing real-world data (e.g., claims, electronic health records, registries).
  • Familiarity with SAS, machine learning, and natural language processing is desirable but not required.
  • Background in biostatistics or related quantitative disciplines.
  • Knowledge of Good Clinical Practice (GCP), quality assurance principles, and regulatory environments.

Preferred:

  • Experience in the pharmaceutical industry.
  • Target trial emulation experience.

#LI-BM1

EEO & Pay Equity Statements

For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is availableย here.

RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

For Applicants in Massachusetts Only:ย It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer.

At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance.

Hiring Salary Range$110,000.00-$130,000.00Employment Type: FULL_TIME