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Internship R Statistical Programmer Jobs (NOW HIRING)

The Principal Statistical Programmer will lead programming activities for one or more studies ... Expertise in R programming. * 6+ years of clinical programing experience * 5+ years of experience ...

Senior Statistical Programmer (Remote) General Information Location: Cary, NC, Remote Organization ... R programming experience preferred. * 2 years of macro programming experience required. * At least ...

Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development ...

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Internship R Statistical Programmer information

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$84.5K

$147.3K

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How much do internship r statistical programmer jobs pay per year?

As of Jun 24, 2026, the average yearly pay for internship r statistical programmer in the United States is $147,292.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,000.00 and $160,000.00 per year, depending on experience, location, and employer.

What is the difference between Internship R Statistical Programmer vs R Statistical Programmer?

AspectInternship R Statistical ProgrammerR Statistical Programmer
Required CredentialsTypically pursuing or recently completed a degree in statistics, biostatistics, or related fieldBachelor's or master's degree in statistics, biostatistics, or related field; professional experience preferred
Work EnvironmentInternship setting, often part-time or temporary, supervised by senior staffFull-time, permanent role within pharmaceutical, biotech, or healthcare industries
Employer & Industry UsageUsed in academic, research, or entry-level industry settingsCommon in clinical research, pharmaceutical companies, and CROs

The main difference between an Internship R Statistical Programmer and an R Statistical Programmer is experience level and employment status. Internships are typically temporary positions for students or recent graduates gaining practical experience, while R Statistical Programmers are full-time professionals responsible for developing and maintaining statistical programming in clinical trials or research projects.

What are the key skills and qualifications needed to thrive as an Internship R Statistical Programmer, and why are they important?

To thrive as an Internship R Statistical Programmer, you need a solid background in statistics, programming with R, and data analysis, usually supported by coursework or a degree in statistics, mathematics, or a related field. Familiarity with RStudio, data visualization libraries (like ggplot2), and version control systems such as Git is typically expected. Attention to detail, problem-solving ability, and effective communication are vital soft skills that help you interpret data and collaborate with team members. These competencies ensure accurate data processing, meaningful statistical insights, and efficient teamwork on research or business projects.

What does an Internship R Statistical Programmer do?

An Internship R Statistical Programmer assists with data analysis, statistical modeling, and data visualization using the R programming language. Interns typically work under the supervision of experienced statisticians or data scientists, helping to clean and manage datasets, write scripts and code in R, and generate reports or graphics for research projects or business analyses. This role provides valuable hands-on experience in statistical programming and is often geared towards students or early-career professionals interested in data science or analytics.

What does a typical day look like for an Internship R Statistical Programmer, and how do interns collaborate with other team members?

As an Internship R Statistical Programmer, your typical day involves writing and testing R scripts to process and analyze data, often under the guidance of experienced programmers or statisticians. You'll participate in team meetings, contribute to code reviews, and work closely with data scientists, biostatisticians, or clinical research teams depending on the industry. Collaboration is key, as you'll frequently discuss analysis plans, clarify data requirements, and troubleshoot code alongside others. This role provides hands-on experience with real-world datasets and fosters growth in both technical and communication skills.
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Principal Statistical Programmer

Principal Statistical Programmer

GSK

Durham, NC • On-site

Full-time

Posted 14 days ago


GlaxoSmithKline rating

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

7th of 71 rated pharmaceutical


Job description

The Principal Statistical Programmer will lead programming activities for one or more studies, ensuring high-quality development, validation, and delivery of complex analysis outputs. Drive technical excellence, innovation, and standards adoption while providing strategic insights into study data. Mentor junior programmers and influence programming approaches through strong technical leadership and communication.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Technical Leadership & Delivery
  • Lead programming for studies, ensuring efficient development and validation of analysis packages.
  • Select appropriate tools/languages and solve complex technical challenges.
  • Identify and implement improvements, including use of AI/ML.
  • Contribute to departmental initiatives and technical strategy.

Quality & Compliance
  • Ensure adherence to standards (e.g., GPP, CDISC) and regulatory requirements.
  • Perform QC on critical outputs and technical documents (e.g., cSDRG, ADRG).
  • Maintain governance and oversee TMF compliance.

Strategy & Innovation
  • Drive adoption of modern technologies, standards, and Agile practices.
  • Provide technical input on programming strategies and study design.
  • Act as SME for emerging tools when needed.

Communication & Mentorship
  • Communicate technical concepts, risks, and timelines clearly to stakeholders.
  • Mentor junior programmers and share best practices internally and externally.

Collaboration & Execution
  • Support sprint planning and project delivery across studies.
  • Collaborate cross-functionally and manage data access appropriately.
  • Support regulatory interactions and contribute to CoE activities.

Accountabilities
  • Serve as Lead Programmer for complex or multiple studies.
  • Ensure quality, compliance, and efficient execution of programming activities.
  • Make data-driven decisions and proactively address risks and issues.

Why You:
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
  • Bachelor's degree in Statistics, Computer Science, or a related field.
  • 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 assistants (e.g., GitHub Copilot, Codex, and Claude) to improve programming efficiency, automation, code quality, and analytical workflows in clinical programming.

Preferred Qualification
If you have the following characteristics, it would be a plus:
  • Strong experience supporting HIV clinical trials and drug development within the pharmaceutical or biotechnology industry.
  • Advanced degree in Statistics, Computer Science, Data Science, or a related discipline.
  • Experience using generative AI tools and coding assistants (e.g., GitHub Copilot, Claude, or Codex) to improve programming productivity and automation.
  • Familiarity with modern software engineering practices, including Git-based workflows, reusable frameworks, and automation pipelines.
  • Experience with R, Python, and open-source analytics tools within regulated clinical development environments.
  • Experience contributing to standards development, process improvement, or digital transformation initiatives.
  • Knowledge of Agile delivery methodologies and collaborative product development approaches.
  • Demonstrated experience leading programming activities for complex clinical studies or multiple projects.
  • Strong understanding of CDISC standards, regulatory expectations, and quality/compliance requirements.
  • Excellent analytical, problem-solving, communication, and stakeholder management skills.
  • Experience mentoring or guiding junior team members

At ViiV Healthcare, our mission is to ensure that the impact of HIV is minimized for individuals and communities worldwide. We are deeply committed to:
  • Patient Focus - Always putting the needs of those living with HIV first.
  • Transparency, Respect, and Integrity - Maintaining open communication, mutual respect, and a high ethical standard in everything we do.
  • Courage and Accountability - Demonstrating bold leadership by making agile, evidence-based decisions and taking responsibility for outcomes.
  • Development and Teamwork - Investing in our team members' growth and building collaborative, impact-driven partnerships internally and externally.

As part of our 30-year legacy of improving lives with HIV, ViiV Healthcare is not just a place to work-it is a community where every team member is empowered to bring their very best to the fight against HIV/AIDS. Our holistic approach extends beyond medicine to supporting sustainable community programs and improving access to care.
#LI-ViiV
#LI-GSK
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.
Why Us?
At ViiV Healthcare, we will not rest until we leave no person living with HIV behind. Until the 40 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV.
We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in 2009, with Shionogi joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.
Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities.
Having a truly inclusive culture where we're all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com
ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
ViiV does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact ViiV's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to ViiV. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and ViiV. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ViiV. ViiV shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, ViiV may be required to capture and report expenses ViiV incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure ViiV's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US