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

micro1 AI

Director of Biostatistics

Cary, NC · Remote

$60 - $100/hr

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets. * Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

micro1 AI

Director of Biostatistics

Durham, NC · Remote

$60 - $100/hr

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets. * Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

UCB

Principal Statistical Methodologist (US)

Raleigh, NC · On-site

Provide statistical consultation on clinical trial design and analysis across multiple development ... Strong statistical programming skills (R preferred; equivalent tools considered). * Sound knowledge ...

Fujifilm

Senior Software Engineer, RIS

Durham, NC

$118K - $156K/yr

This position is intended to be a member of the engineering team, developing software for medical ... Design and implement product features from internal and external customer requirements and clinical ...

RTI International

Senior Research Statistician

Raleigh, NC · On-site

$84K - $104K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

MMS

Study Design Statistician (US)

Raleigh, NC · On-site

... 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 ...

RTI International

Senior Research Statistician

Raleigh, NC · On-site +1

$84K - $104K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

RTI International

Senior Research Statistician

Raleigh, NC · On-site

$84K - $104K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

RTI International

Senior Research Statistician

Durham, NC · On-site

$84K - $103K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

RTI International

Senior Research Statistician

Durham, NC

$84K - $103K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

RTI International

Senior Research Statistician

Raleigh, NC

$84K - $104K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... clinical research, HEOR, epidemiology, or related consulting environments. * Advanced programming proficiency in R is required; experience with STATA, SAS, or Bayesian software is preferred.

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Showing results 21-40

All JobsClinical R Programmer JobsClinical R Programmer Jobs in Apex, NC

Clinical R Programmer information

See Apex, NC salary details

$18

$49

$78

How much do clinical r programmer jobs pay per hour?

As of Aug 18, 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 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.

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:

Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in Apex, NC as of August 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $102,660 per year, or $49.4 per hour.

Director of Biostatistics

micro1 AI

Cary, NC • Remote

$60 - $100/hr

Part-time

Posted 11 days ago

Job description

Role Title: Biostatistician


Role Type: Contractor


Location: Remote


micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
  2. Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
  3. Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
  4. Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
  5. Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
  6. Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.


Preferred Qualifications

  1. MS or PhD in biostatistics, statistics, or epidemiology.
  2. 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
  3. Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
  4. Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
  5. Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
  6. Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
  7. Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.


Compensation Structure

Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.


Start Timeline & Availability

We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.

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