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Clinical Sas Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Provide endtoend statistical programming support for clinical studies from study setup through ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$98K - $273K/yr

Provide endtoend statistical programming support for clinical studies from study setup through ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

Duke University

Biostatistician III

Durham, NC · On-site

Demonstrated experience contributing to clinical trials, clinical research studies, or other ... Thorough experience with R and SAS programming. * Strong written and verbal communication skills ...

Duke University

Biostatistician III

Durham, NC · On-site

Demonstrated experience contributing to clinical trials, clinical research studies, or other ... Thorough experience with R and SAS programming. * Strong written and verbal communication skills ...

Gilead

Senior Manager, Statistical Programming

Raleigh, NC · On-site

$169K - $219K/yr

Works collaboratively with Clinical Development staff to meet project deliverables and timelines ... GCP, ICH) * Extensive experience with statistical programming using the SAS software including ...

Gilead

Senior Manager, Statistical Programming

Raleigh, NC · On-site

$169K - $219K/yr

Works collaboratively with Clinical Development staff to meet project deliverables and timelines ... GCP, ICH) * Extensive experience with statistical programming using the SAS software including ...

INC Research

Senior Biostatistician

Raleigh, NC · On-site

Moderate experience in clinical trials or equivalent combination of education and experience. 2. Experience in SAS programming. Excellent knowledge of statistical theory including experimental design ...

INC Research

Senior Biostatistician

Raleigh, NC · On-site

Moderate experience in clinical trials or equivalent combination of education and experience. 2. Experience in SAS programming. Excellent knowledge of statistical theory including experimental design ...

MMS

Study Design Statistician (US)

Raleigh, NC · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Experience in SAS and/ or R statistical software packages. * Experience in study design and ...

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Showing results 21-40

All JobsClinical Sas JobsClinical Sas Jobs in Raleigh, NC

Clinical Sas information

See Raleigh, NC salary details

$18

$52

$78

How much do clinical sas jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical sas in Raleigh, NC is $52.53, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $66.11 per hour, depending on experience, location, and employer.

What is a clinical SAS?

Clinical SAS professionals are specialists who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. They play a critical role in ensuring data integrity and compliance with regulatory standards by generating statistical reports, tables, listings, and graphs for clinical studies. These professionals often collaborate with biostatisticians, clinical researchers, and data managers to support the drug development and approval process.

What are the key skills and qualifications needed to thrive as a clinical SAS programmer?

To thrive as a Clinical SAS Programmer, you need expertise in SAS programming, a solid understanding of clinical trial data, and a degree in life sciences, statistics, or a related field. Familiarity with CDISC standards (SDTM/ADaM), clinical data management systems, and regulatory submission requirements is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills ensure accurate data analysis and reporting, which are critical for regulatory compliance and successful clinical trial outcomes.

What are some common challenges faced by clinical SAS programmers when working on clinical trial data?

Clinical SAS programmers often encounter challenges such as managing large and complex datasets from multiple sources, ensuring strict compliance with regulatory standards (like CDISC, SDTM, and ADaM), and meeting tight project deadlines. They must also collaborate closely with biostatisticians, data managers, and clinical teams to ensure data accuracy and consistency. Staying updated with evolving industry standards and software updates is crucial, as is maintaining clear documentation to support regulatory submissions.

What is the difference between Clinical Sas vs Clinical Data Manager?

AspectClinical SasClinical Data Manager
Required CredentialsBiostatistics, SAS certification, or related trainingBiostatistics, data management certifications, or related degrees
Work EnvironmentStatistical analysis, programming, and reporting in clinical trialsData collection, validation, and database management in clinical studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research organizations

Clinical Sas professionals focus on statistical analysis and programming using SAS software to interpret clinical trial data. In contrast, Clinical Data Managers oversee data collection, validation, and database management to ensure data quality. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

What are popular job titles related to Clinical Sas jobs in Raleigh, NC?

For Clinical Sas jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Sas jobs in Raleigh, NC look for?

The top searched job categories for Clinical Sas jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Sas jobs?

Cities near Raleigh, NC with the most Clinical Sas job openings:

Clinical Sas jobs near you
Infographic showing various Clinical Sas job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $109,261 per year, or $52.5 per hour.

Principal Statistical Programmer

IQVIA

Durham, NC • On-site

$98K - $273K/yr

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Position Summary

We are seeking a Principal Statistical Programmer to provide full endtoend statistical programming support across clinical development programs. This role requires deep technical expertise, leadership, and handson delivery, covering SDTM, ADaM, TLF development, and regulatory submission support. The Principal Statistical Programmer will serve as a subject matter expert, ensure highquality deliverables, and contribute to programming standards and best practices.

Key Responsibilities

  • Provide endtoend statistical programming support for clinical studies from study setup through submission

  • Lead and perform development and validation of:

    • SDTM datasets

    • ADaM datasets

    • Tables, Listings, and Figures (TLFs)

  • Ensure all deliverables are compliant with CDISC standards and regulatory requirements

  • Support regulatory submissions (e.g., FDA, EMA), including define.xml, submissionready datasets, and reviewer's guides

  • Serve as a Principallevel programmer, providing technical leadership and guidance to other programmers as needed

  • Contribute to and help maintain programming standards, macros, and validation processes

  • Review and approve programming deliverables to ensure accuracy, consistency, and quality

  • Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams

  • Proactively identify risks and propose efficient, compliant solutions within timelines

Required Qualifications

  • Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field

  • Extensive experience as a statistical programmer, with demonstrated Principallevel responsibilities

  • Strong handson experience with:

    • SDTM and ADaM dataset development

    • TLF programming

    • Regulatory submission deliverables

  • Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros

  • Indepth knowledge of CDISC standards, regulatory guidelines, and submission requirements

  • Proven ability to manage complex studies independently from start to finish

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 $98,200.00 - $273,200.00. 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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