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Clinical Sas Jobs in Raleigh, NC (NOW HIRING)

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 ...

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.

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.

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.

Senior Statistician

Durham, NC · On-site +1

$84K - $103K/yr

Develop, evaluate, and run Statistical Analysis System (SAS) programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, Clinical Data ...

Senior Statistician

Durham, NC

$84K - $103K/yr

Develop, evaluate, and run Statistical Analysis System (SAS) programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, Clinical Data ...

About the job The SAS Health Care Center (HCC) is looking for a Medical Office Administrator to ... a clinical staff member. Must be able to handle multiple lines and issues concurrently.

About the job The SAS Health Care Center (HCC) is looking for a Medical Office Administrator to ... a clinical staff member. Must be able to handle multiple lines and issues concurrently.

About the job The SAS Health Care Center (HCC) is looking for a Medical Office Administrator to ... a clinical staff member. Must be able to handle multiple lines and issues concurrently.

About the job The SAS Health Care Center (HCC) is looking for a Medical Office Administrator to ... a clinical staff member. Must be able to handle multiple lines and issues concurrently.

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... such as SAS, R, SPSS, NVivo, or Atlas.ti. Scientific Contribution * Participate in protocol ...

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... such as SAS, R, SPSS, NVivo, or Atlas.ti. Scientific Contribution * Participate in protocol ...

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

Demonstrate a proven track record of a minimum of 8 years in clinical project management, preferably within the healthcare industry and with experience in SAS solutions. * Possess a comprehensive ...

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 ...

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 ...

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 ...

Senior Statistician

Durham, NC · On-site +1

$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 information

See Raleigh, NC salary details

$18

$52

$78

How much do clinical sas jobs pay per hour?

As of Aug 25, 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 cities near Raleigh, NC are hiring for Clinical Sas jobs?

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

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, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $109,261 per year, or $52.5 per hour.

Senior Programmer Analyst- Remote, US

Durham, NC • On-site


Fortrea
10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 74 rated research

People enjoy working here

Good employer

Respectful managers


$80K - $95K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

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


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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