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

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 ...

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 · On-site

$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 ...

Duke University

Research Technician II

Durham, NC · On-site

$19.06 - $28.85/hr

... clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate ... Some basic computer science background (python or R programming) would be useful. Anticipated Pay ...

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Clinical R Programmer information

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$62

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How much do clinical r programmer jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for clinical r programmer in Raleigh, NC is $62.97, according to ZipRecruiter salary data. Most workers in this role earn between $52.12 and $71.25 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 Raleigh, NC? For Clinical R Programmer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Raleigh, NC look for? The top searched job categories for Clinical R Programmer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical R Programmer jobs? Cities near Raleigh, NC with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you
Principal Biostatistician FSP, Late Phase

Principal Biostatistician FSP, Late Phase

IQVIA

Durham, NC • Remote

$115K - $243K/yr

Full-time

Posted 20 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 208 rated it services

Job description

Job Level: FSP Principal Biostatistician, Late Phase

Location: Home-based in the U.S. or Canada

Why DSSS?

Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market.

Job Summary:

The Principal Biostatistician is responsible for providing statistical support for pharmaceutical clinical trials in patients.

Additional Benefits:

  • Home-based remote working opportunities.
  • Work/life balance as well as flexible schedules.
  • Collaborating with motivated, high-performance, statistical and research teams.
  • Technical training and tailored development curriculum.
  • Research opportunities that match your unique skillset.
  • Promising career trajectory.
  • Job stability: long-term engagements and re-deployment opportunities.
  • Focus on bringing new therapies to market rather than project budgets and change orders.
  • Experience with regulatory submissions.
  • Engaging, fast-paced environment.
  • Good work-life balance.

Job Responsibilities:

  • Collaborate with multi-disciplinary project teams to establish project objectives and timelines.
  • Author statistical analysis plans.
  • Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
  • Author or review analysis dataset and TLF specifications
  • Validation programming of efficacy analysis datasets plus tables, listings, and figures (TLF)
  • Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming/validation of tables, listings, and figures for safety, etc.
  • Interpret study results and review reports of study results for accuracy.
  • Support exploratory analyses.
  • Participate in IND or NDA activities.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Contribute to clinical study reports and other regulatory documents, e.g. NDA, DSURs, Briefing Documents, ISS, ISE, SCE (Summary of Clinical Efficacy), SCS (Summary of clinical Safety).

Qualifications

  • PhD in Statistics, Biostatistics, or related field with 3+ years of industry experience.
  • MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
  • At least 2 years in Phase 2/3 clinical trial experience.
  • Demonstrated ability to work pro-actively and independently.
  • Able to effectively communicate ideas and collaborate with cross-functional teams
  • Ability to use R or SAS to perform efficacy and safety analyses and validate important data derivations when necessary.
  • Support of various regulatory submissions
  • Understanding of relevant FDA guidance, ICH GCP, ICH E9 plus general knowledge of industry practices and standards.
  • Experience in validation/programming of ADAM and TLF
  • Experience with CDISC, including SDTM, ADAM, CDASH
  • Solid understanding of estimands and multiple imputation methods.

Desired Experience:

  • Supporting written communications with regulators.
  • 1+ years of experience with immunology therapeutic area.
  • Bayesian methods

#LI-Remote

#LI-NITINMAHAJAN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $115,900.00 - $243,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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