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

Fortrea

Senior Programmer Analyst- Remote, US

Durham, NC · On-site

$80K - $95K/yr

Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming. * Lead the development of visual analytics ...

IQVIA

Senior Statistical Programmer

Durham, NC · On-site

$88K - $220K/yr

Conduct statistical programming work of clinical data using SAS Software. * Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with ...

IQVIA LLC

Senior Statistical Programmer

Durham, NC · On-site

$88 - $221/hr

Conduct statistical programming work of clinical data using SAS Software. * Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with ...

micro1 AI

Director of Biostatistics

Raleigh, NC · Remote

$60 - $100/hr

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets. * Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

micro1 AI

Director of Biostatistics

Cary, NC · Remote

$60 - $100/hr

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets. * Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

micro1 AI

Director of Biostatistics

Durham, NC · Remote

$60 - $100/hr

Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets. * Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.

LivaNova

Statistical Programmer II

Raleigh, NC · On-site

$90K - $100K/yr

Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues. * Develop, validate, and maintain SAS programs in accordance ...

NCBiotech

Principal Statistician

Durham, NC · On-site

$110 - $150/hr

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

PSI CRO

Principal Statistician

Durham, NC

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

PSI CRO

Principal Statistician

Durham, NC · On-site +1

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

PSI CRO

Principal Statistician

Durham, NC

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

PSI CRO

Senior Statistician

Durham, NC · On-site

$84K - $103K/yr

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

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Clinical Sas Programmer information

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How much do clinical sas programmer jobs pay per hour?

As of Aug 25, 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.

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.

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.

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 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.

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. Skills in SAS programming, knowledge of regulatory requirements, and experience with electronic data capture systems increase employability in this field.

Is a clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the pharmaceutical and healthcare industries, focusing on data analysis and reporting using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience in clinical trial processes. The role typically requires strong analytical skills and knowledge of regulatory standards such as GCP and FDA guidelines.

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.
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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 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $109,254 per year, or $52.5 per hour.

Senior Programmer Analyst- Remote, US

Fortrea

Durham, NC • On-site

$80K - $95K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 74 rated research

Job description

Job Overview:

Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and reconciliations. Perform any postproduction changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, SAS Datasets etc., Conduct Peer Review/Quality control of study design for assigned projects.

    Summary of Responsibilities:

    • Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming.
    • Lead the development of visual analytics dashboard using tools like Spotfire/Tableau.
    • Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software according to Fortrea SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices.
    • Perform any post-production changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc.,
    • With assistance, meet with Data Manager on assigned projects to discuss contractual obligations and timelines.
    • Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to EDC tools or SAS programming.
    • Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets.
    • Develop/validate Custom/Complex SDTM domains and efficiently handle external data and data reconciliations.
    • Develop and implement SDTM automation/standardization and best programming practices across projects to enhance quality and productivity.
    • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
    • Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.
    • Participate in the ongoing review of the processes used to ensure adaptation of best practices.
    • Conduct Peer Review/Quality control of study design for assigned projects.
    • Able to work independently and take initiative to accept new challenges in Clinical Programming Applications, also participate in the validation of new or updates to software.
    • Maintain awareness of new developments in EDC products which may be applied to improve the efficient use of these systems.
    • Resource forecasting and allocate activities to the team members on the project.
    • Proactively identify trends, generate reports/metrics, or demonstrate programming processes to sponsors/auditors (if required), assist with the design of ECRFs and other study documents.
    • And all other duties as needed or assigned

    Qualifications (Minimum Required):

    • University / college degree (life sciences, health sciences, information technology or related subjects preferred).
    • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor's degree.
    • Fluent in English, both written and verbal.
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Experience (Minimum Required):

    • 5 to 8 years of relevant work experience to include data management and database support or SAS Programming or Spotfire or Tableau development.
    • Good problem-solving skills and a proactive approach.
    • Good oral and written communication skills.
    • Basic knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.
    • Demonstrated ability to work in a team environment.
    • Demonstrated ability to work independently under supervision.
    • Proven interpersonal skills.

    Physical Demands/Work Environment:

    • Office work environment.
    Pay Range:$80,000-$95,000 USDBenefits:All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.Application Deadline:09/01/2026#LI Remote

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