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Clinical Sas Jobs in Raleigh, NC (NOW HIRING)

Worldwide Clinical Trials

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 ...

Worldwide Clinical Trials

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 ...

SAS

Medical Office Administrator

Cary, NC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

SAS

Medical Office Administrator

Cary, NC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

SAS

Medical Office Administrator

Cary, NC

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

Open Sas

Medical Office Administrator

Cary, NC · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Retirement

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 ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Retirement

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 ...

Pluto Health

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Fortrea

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Fortrea

Associate Clinical Data Manager

Durham, NC

  • 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 ...

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Showing results 1-20

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 Aug 12, 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 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 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 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 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 2% As Needed, 72% Full Time, 19% Part Time, and 7% 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.

Statistical Programmer / Clinical Data Architect

Volto USA

Raleigh, NC • On-site

Contractor

Re-posted 11 days ago

Job description

Job Description: Local to Raleigh, NC  Only!
Role Overview
We are seeking a highly experienced Senior Statistical Programmer / Clinical Data Architect with 15+ years of expertise in clinical data programming, CDISC standards, and cloud-based analytics platforms. The ideal candidate will lead end-to-end clinical data workflows, regulatory submissions, and modern data platform transformations in GxP-regulated environments.
This role requires strong domain expertise in SDTM, ADaM, regulatory submissions, and SAS/Python/R programming, combined with experience in cloud platforms (AWS/Azure) and clinical data modernization initiatives.
________________________________________
Key Responsibilities
Clinical Data Programming & Regulatory Submissions
•       Design, develop, and validate SDTM and ADaM datasets in compliance with CDISC standards
•       Lead generation of define.xml, aCRF/eCRF annotations, and submission-ready deliverables
•       Develop and optimize automated submission pipelines for FDA and global regulatory authorities
•       Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ICH E6 guidelines
Data Engineering & Automation
•       Architect and implement end-to-end clinical data pipelines using SAS, Python, and R
•       Develop reusable SAS macro libraries and automation frameworks
•       Build scalable data pipelines including modern formats (JSON/XPT alternatives)
•       Drive migration from legacy systems to modern data architectures
Cloud & Platform Engineering
•       Lead implementation and optimization of SAS Viya platforms on AWS/Azure
•       Manage cloud infrastructure components (EKS, EC2, EFS, FSx, Databricks, etc.)
•       Implement FinOps practices for cost governance and optimization
•       Evaluate and onboard next-gen analytics platforms (e.g., Databricks)
Leadership & Stakeholder Management
•       Lead cross-functional teams across US, UK, and offshore locations
•       Collaborate with clinical, statistical, regulatory, and IT stakeholders
•       Drive Agile delivery and sprint planning for data and platform initiatives
•       Manage vendor relationships, tool selection, and licensing strategies
Compliance & Governance
•       Ensure adherence to regulatory and audit requirements (FDA, OCC, SOX, Basel III as applicable)
•       Maintain audit-ready documentation and validation processes
•       Implement data governance, traceability, and reproducibility standards
________________________________________
Required Qualifications
•       Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or related field
•       15+ years of experience in statistical programming and clinical data management
•       Strong expertise in:
o       SAS (Base, Macro, SQL, ODS, STAT, Graph)
o       CDISC standards (SDTM, ADaM, define.xml)
o       Regulatory submissions (FDA, global agencies)
•       Hands-on experience with:
o       Python (Pandas) and/or R (admiral, Shiny)
o       Cloud platforms (AWS/Azure)
•       Strong understanding of GxP and clinical compliance frameworks
________________________________________
Preferred Qualifications
•       Experience with SAS Viya architecture and administration
•       Familiarity with Databricks, DBT, or modern data engineering tools
•       Knowledge of CI/CD tools (Jenkins, Git)
•       Experience in financial/regulatory environments (Basel III, CCAR, OCC) is a plus
•       AWS or cloud certifications
________________________________________
Key Skills
•       Clinical Data Standards: SDTM, ADaM, CDISC
•       Programming: SAS, Python, R, SQL
•       Cloud: AWS, Azure
•       Tools: Pinnacle 21, Git, Jenkins, Power BI, Grafana
•       Methodologies: Agile, DevOps, Data Governance