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

MMS

Senior Biostatistician - Remote (US)

Raleigh, NC · On-site

Strong SAS programming, SAS base, SAS macro experience. * Thorough knowledge and understanding of clinical data preferred. * Strong experience with data and production of TLGs. * Excellent scientific ...

Fortrea

Associate Clinical Data Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Design, SAS Programming, Statistics, and PK to ensure that all deliverables are planned and ... Provides leadership, mentorship, and coaching in DM related clinical trial processes to the ...

Duke University

Biostatistician III

Durham, NC · On-site

  • Medical

  • Dental

  • Retirement

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

  • Medical

  • Dental

  • Retirement

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

Fortrea

Sr. Clinical Data Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ... Design, SAS Programming, Statistics, and PK to ensure that all deliverables are planned and ...

New

Fortrea

Senior Clinical Data Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ... Design, SAS Programming, Statistics, and PK to ensure that all deliverables are planned and ...

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

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 ...

Gilead

Senior Manager, Statistical Programming

Raleigh, NC · On-site

$169K - $219K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

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

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Showing results 21-40

All JobsClinical Sas Programmer JobsClinical Sas Programmer Jobs in Raleigh, NC

Clinical Sas Programmer information

See Raleigh, NC salary details

$18

$52

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How much do clinical sas programmer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical sas programmer 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 programmer?

A Clinical SAS Programmer is a professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and medical research industries. Their main responsibilities include creating programs to clean, organize, and analyze clinical data, generating summary tables and listings, and ensuring the accuracy and compliance of data for regulatory submissions. They work closely with biostatisticians, data managers, and clinical researchers to support drug development and approval processes.

Is a clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the pharmaceutical and healthcare industries, focusing on analyzing clinical trial data using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience in data management and statistical analysis. The role typically requires strong programming skills and knowledge of regulatory standards such as GxP and CDISC.

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

To thrive as a Clinical SAS Programmer, you need strong programming skills in SAS, a solid understanding of clinical trial data, and often a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (SDTM, ADaM), clinical data management systems, and regulatory submission processes is typically required. Attention to detail, problem-solving abilities, and effective communication skills help you collaborate with cross-functional teams and ensure data quality. These skills are vital for ensuring accurate data analysis and compliance with industry regulations in clinical research.

Are Clinical SAS Programmers in demand?

Clinical SAS Programmers are in high demand due to the ongoing need for data analysis and reporting in clinical trials. Their skills in SAS programming, regulatory compliance, and understanding of clinical research processes make them valuable in pharmaceutical and biotech industries, with job opportunities often available in both contract and permanent roles.

What is the difference between Clinical Sas Programmer vs Clinical Data Analyst?

AspectClinical Sas ProgrammerClinical Data Analyst
Required CredentialsBachelor's in IT, Life Sciences, or related; SAS certification often preferredBachelor's in Statistics, Data Science, or related; often requires statistical or data analysis certifications
Work EnvironmentPharmaceutical or CRO settings, working with SAS software to develop datasets and reportsResearch or clinical settings, analyzing clinical data to generate insights and reports
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, research organizations, healthcare providers

While both roles involve working with clinical data, Clinical Sas Programmers focus on programming, data manipulation, and report generation using SAS software. Clinical Data Analysts primarily analyze data to interpret results and support decision-making. Both roles require strong analytical skills but differ in their core responsibilities and technical focus.

What are 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, ensuring data integrity, and adhering to strict regulatory guidelines. They must also collaborate closely with biostatisticians and data managers to resolve data discrepancies and interpret study protocols accurately. Timely delivery of high-quality statistical outputs, such as tables, listings, and figures, is critical, often under tight deadlines. Effective communication and attention to detail are essential to overcome these challenges and deliver reliable results.

What is the salary of clinical SAS programmer?

The salary of a clinical SAS programmer typically ranges from $70,000 to $110,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced programmers with advanced skills can earn higher salaries, especially in competitive markets or with specialized knowledge of clinical trial data analysis.

What is a SAS clinical programmer?

As a SAS clinical programmer, your primary responsibilities are the management and analysis of large datasets of information from clinical trials. Your job duties include using and programming the statistical analysis system, or SAS software suite, to develop tables and reports about the interdependencies of data points and the efficacy of trial-phase clinical therapies. The qualifications for a career as a SAS clinical programmer are a bachelor’s degree in statistics or computer science and experience in the pharmaceutical or clinical industries. You must develop strong SAS technical skills and problem-solving skills to succeed in a career as a SAS clinical programmer.

More about Clinical Sas Programmer jobs
What are the most commonly searched types of Clinical Sas Programmer jobs in Raleigh, NC? The most popular types of Clinical Sas Programmer jobs in Raleigh, NC are:
What are popular job titles related to Clinical Sas Programmer jobs in Raleigh, NC? For Clinical Sas Programmer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Sas Programmer jobs in Raleigh, NC look for? The top searched job categories for Clinical Sas Programmer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Sas Programmer jobs? Cities near Raleigh, NC with the most Clinical Sas Programmer job openings:
Clinical Sas Programmer jobs near you
Infographic showing various Clinical Sas Programmer job openings in Raleigh, NC as of August 2026, with employment types broken down into 77% Full Time, 6% Part Time, and 17% Contract. Highlights an 61% In-person, 6% Hybrid, and 33% Remote job distribution, with an average salary of $109,254 per year, or $52.5 per hour.

Senior Principal Programmer, Raleigh, NC

UCB

Raleigh, NC • On-site

Full-time

Posted 6 days ago

Job description

Make your mark for patients
We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in Raleigh, NC or Atlanta, GA.
About the role
You will help clinical programming teams move to and work confidently within UCB's modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.
Who you'll work with
You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.
What you'll do
You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
Interested? For this position you'll need the following education, experience and skills:
You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.
You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.
You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.
Unless explicitly stated in the description, this role is hybrid with 40% of your time spent in the office, regardless of your current contractual agreement. If your current working arrangements differ, please contact your Talent Partner to discuss before submitting your application.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Requisition ID: 93699
Recruiter: Kevin Ross
Hiring Manager: Tim Williams
Talent Partner: Natacha Tassier
Job Level: MM I
Please consult HRAnswers for more information on job levels.

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