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Assistant R Statistical Programmer Jobs in Cary, NC

UCB

Principal Statistician, Raleigh, NC

Raleigh, NC · On-site

Proficient in statistical programming (e.g., SAS or R) and simulation tools * Strong stakeholder ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

UCB

Principal Statistician, Raleigh, NC

Raleigh, NC · On-site

Proficient in statistical programming (e.g., SAS or R) and simulation tools * Strong stakeholder ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

Contemporaries

Be Seen First

Data Scientist

Durham, NC · Remote

$51 - $58/hr

... * Assist with peer-reviewed manuscript development, including data analysis, technical writing ... statistical programming, or computational research support * Strong experience using the R ...

Duke University

Biostatistician II

Durham, NC · On-site

... statistical testing, and modeling. * Write code (e.g., R, SAS) to design analytic datasets, validate outputs, identify errors, and ensure data integrity. * Perform advanced programming tasks such as ...

Clever Devices Ltd.

Associate

Apex, NC · On-site

$70K - $75K/yr

... * Assist in writing programs to cleanse data with the purpose of integrating it into operations in ... Basic and educational level understanding of statistical programming (i.e. Python, R, SAS, MATLAB ...

Alimentiv

Statistician

Raleigh, NC · Remote

Carry out statistical analyses and provide direction to programmers, using standard software ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...

Alimentiv

Statistician

Raleigh, NC

Carry out statistical analyses and provide direction to programmers, using standard software ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...

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Assistant R Statistical Programmer information

See Cary, NC salary details

$78.3K

$136.5K

$230.7K

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

As of Jun 7, 2026, the average yearly pay for assistant r statistical programmer in Cary, NC is $136,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,800.00 and $148,200.00 per year, depending on experience, location, and employer.

What is the difference between Assistant R Statistical Programmer vs Data Analyst?

AspectAssistant R Statistical ProgrammerData Analyst
Required SkillsProficiency in R, basic statistical knowledge, programming skillsData manipulation, visualization, statistical analysis, often using R or Excel
Work EnvironmentClinical research, pharmaceutical, or biotech industriesBusiness, marketing, finance, healthcare sectors
CertificationsOften requires a degree in statistics, biostatistics, or related fieldsDegree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common

While both roles involve data analysis and programming skills, the Assistant R Statistical Programmer primarily supports clinical trials and pharmaceutical research, focusing on statistical programming in R. Data Analysts work across various industries analyzing data to inform business decisions. The roles share similar educational backgrounds but differ in industry focus and specific job functions.

What are the most commonly searched types of R Statistical Programmer jobs in Cary, NC? The most popular types of R Statistical Programmer jobs in Cary, NC are:
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Assistant R Statistical Programmer jobs near you
FSP Principal Biostatistician, Safety Analytics

FSP Principal Biostatistician, Safety Analytics

IQVIA, Inc.

Durham, NC • On-site

Full-time

Posted 6 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

53rd of 203 rated it services

Job description

Job: FSP Principal Biostatistician, Safety Analytics
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 Phase 1, 2 and 3 pharmaceutical clinical trials in patients, focusing on safety endpoints and outcomes.
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:
  • Support Safety Analytics with ADaM/TFL standard development for Hypersensitivity, Injection/Infusion Site Reaction or other safety deliverables.
  • Support Safety Analytics and the study team on the delivery of Patient Profile display for Hepatic or other areas.
  • Provide ADaM/TFL/interactive package review support for the Safety Analytics team supported portfolio deliveries, including cross-checks between interactive outputs and TFLs.
  • Interrogating root cause of issues identified during ADaM/TFL/Interactive package review
  • Providing statistical leadership and support for safety analyses for Phase 1/2/3 trials.
  • Collaborate with multi-disciplinary project teams to establish project objectives and timelines.
  • Participating in study design discussions, including protocol development
  • Write the statistical sections of clinical trial protocols.
  • Reviewing CRFs, data review guidelines, and related study documentation to ensure statistical and safety considerations are appropriately addressed.
  • Developing and reviewing statistical analysis plans and TFL templates.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
  • Contribute to clinical study reports and other regulatory documents, e.g. NDA, DSURs, Briefing Documents, ISS, ISE, etc.
  • Serving as an unblinded DMC statistician across multiple studies, ensuring compliance with sponsor and regulatory requirements.
  • Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming/validation of tables, listings, and figures.
  • Perform exploratory safety analyses
  • Perform validation of analysis variables and statistical outputs
  • Interpret study results and review reports of study results for accuracy.
  • Present, communicate and interpret safety analyses to study teams
  • Support exploratory analyses.
  • Participate in pre-IND or NDA activities.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • PhD in Statistics, Biostatistics, or related field with 3+ years industry experience.
  • MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
  • At least 2 years of Phase 1, 2 and 3 clinical trial experience.
  • Strong experience reviewing ADaM datasets and TFLs (standard and customized output review).
  • Ability to follow data specifications and programming specifications and provide clear, actionable review comments.
  • Able to investigate and troubleshoot mismatches between tools/outputs (e.g., Spotfire vs. SAS TFL) by interrogating programs to identify root cause and errors.
  • Strong communication and time management: provide realistic timeline estimates, flag risks/delays early, and ask the right questions to move work forward.
  • R/SAS programming skills
  • Demonstrated ability to work pro-actively and independently.
  • Able to effectively communicate his/her ideas and to manage programmers in a constructive manner.
  • Understanding of ICH GCP, ICH E9 plus general knowledge of industry practices and standards.
  • Experience with CDISC, including SDTM, ADAM, CDASH

Desired Experience:
  • Leading DSBM or DMC for biostatistics

#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 at https://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 $111,000.00 - $309,000.00. 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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Benefits

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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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