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Clinical Sas Jobs (NOW HIRING)

Integrated Resources INC

SAS Programming

Madison, NJ · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Performs all SAS programming required for clinical trial analysis and reporting; Ensures that activities and ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA · On-site

$145K - $156K/yr

Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS). * Comprehensive understanding of clinical trial processes, data flow, and clinical trial data ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Knowledge of R programming in clinical trials Familiarity of the drug development process. Knowledge of CDISC standards and electronic submission requirements. Strong SAS and SAS Macro language ...

CICONIX, LLC

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

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Clinical Sas information

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How much do clinical sas jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for clinical sas in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What is the difference between SAS and clinical SAS?

Clinical SAS refers to the use of SAS software specifically for clinical trial data analysis and reporting, often following industry regulations like 21 CFR Part 11. SAS as a broader tool is used across various industries for data management, analytics, and reporting, while clinical SAS involves specialized knowledge of clinical data standards and regulatory requirements. Clinical SAS professionals typically focus on clinical trial datasets, programming, and validation processes within the pharmaceutical and biotech sectors.

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 jobs pay 2000 a day?

Clinical SAS (Statistical Analysis System) professionals, such as senior biostatisticians or clinical data consultants, can earn around $2,000 per day, especially when working on high-stakes clinical trials or consulting projects. These roles typically require advanced statistical skills, industry experience, and often involve contract or consulting work with specialized knowledge of clinical research and regulatory standards.

Is 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 steady employment, competitive salaries, and opportunities for skill development in data management and regulatory compliance. The role typically requires knowledge of SAS programming, clinical trial processes, and relevant certifications.

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.

How hard is it to get a job at SAS?

Getting a Clinical SAS job typically requires relevant experience in clinical research, statistical analysis, or data management, along with proficiency in SAS software. Candidates often need a strong educational background, certifications, and familiarity with industry regulations, making the hiring process competitive but achievable with the right skills and qualifications.

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 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 Clinical SAS professionals?

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.
More about Clinical Sas jobs
What cities are hiring for Clinical Sas jobs? Cities with the most Clinical Sas job openings:
What states have the most Clinical Sas jobs? States with the most job openings for Clinical Sas jobs include:
What job categories do people searching Clinical Sas jobs look for? The top searched job categories for Clinical Sas jobs are:
Clinical Sas jobs near you
Infographic showing various Clinical Sas job openings in the United States as of June 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 78% In-person, 11% Hybrid, and 11% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

SAS Viya Developer

Thunderhawk Technology Partners

Raleigh, NC

Other

Posted 8 days ago

Job description

Position: SAS Viya Developer
Location: Raleigh, NC
Duration: Contract
Role Overview
  • We are seeking a highly experienced SAS Viya devloper with experience between 5 to 10 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:
  • SAS (Base, Macro, SQL, ODS, STAT, Graph)
  • CDISC standards (SDTM, ADaM, define.xml)
  • Regulatory submissions (FDA, global agencies)
  • Hands-on experience with:
    • Python (Pandas) and/or R (admiral, Shiny)
    • Cloud platforms (AWS/Azure)
  • Strong understanding of GxP and clinical compliance frameworks

Apply