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Clinical Sas Jobs (NOW HIRING)

Extensive programming experience in a clinical trial environment (CRO/Pharma). * Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. * In-depth knowledge of CDISC standards and regulatory submission ...

Clinical SAS Technical Lead / Biometrics Systems Location: Alameda, CA (Hybrid, 2-3 days/week onsite) Position Type: Fulltime * This role will be a critical part of our managed services program (MSP ...

NOT CLINICAL Experience with administration and tuning for SAS Grid Manager/SAS Platform Expertise in setup of queues, prioritization, manage jobs and thresholds Experience with troubleshooting and ...

NOT CLINICAL • Experience with administration and tuning for SAS Grid Manager/SAS Platform Expertise in setup of queues, prioritization, manage jobs and thresholds Experience with troubleshooting ...

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: Develop SAS programs for tables, listings, and ...

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements: Key Responsibilities: • Develop SAS programs for tables, listings ...

Extensive programming experience in a clinical trial environment (CRO/Pharma). Expertise in SAS ... BASE, SAS/STAT, and SAS/MACRO. In-depth knowledge of CDISC standards and regulatory submission ...

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: • Develop SAS programs for tables, listings ...

Medpace is a full-service clinical contract research organization (CRO) that provides clinical ... They are currently seeking an experienced SAS Programmer to join their Biostatistics team to write ...

Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical development services. They are seeking an Entry Level SAS Programmer to join their Biostatistics ...

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Clinical Sas information

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$54

$80

How much do clinical sas jobs pay per hour?

As of Jun 12, 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:
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.

Clinical SAS Programmer

Interon IT Solutions

Chantilly, VA • Remote

Contractor

Posted 2 days ago


Job description

#W2 Role

Job Title: Clinical SAS Programmer

No of positions- 2

Location- Remote
Experience Required:6+ Years
Education: Bachelor’s degree in Computer Science, Computer Engineering, or related technical field

 

Job Summary

We are seeking a Clinical SAS Programmer with strong experience in SAS programming and CDISC standards within a regulatory environment. The ideal candidate will be responsible for creating and validating SDTM domains and ADaM datasets, developing mapping specifications, and supporting clinical data programming activities with accuracy and compliance.

Key Responsibilities

  • Develop and validate specifications for creating SDTM domains from raw/source clinical data.
  • Create and validate CDISC-compliant SDTM domains and ADaM datasets using SAS.
  • Prepare mapping specifications from CRF and other raw data sources to appropriate SDTM domains.
  • Develop specifications to map SDTM datasets to ADaM datasets.
  • Write clear and detailed programming instructions for complex data derivations.
  • Perform dataset validation and quality checks to ensure regulatory compliance and data integrity.
  • Develop SAS macros and reusable programs to improve efficiency and streamline workflow.
  • Apply advanced SAS programming techniques for custom clinical data programming needs.
  • Work effectively in a dynamic environment and adapt quickly to changing project requirements.

Required Qualifications

  • Bachelor’s degree in Computer Science, Computer Engineering, or a related technical field.
  • 4+  years of experience in clinical SAS programming.
  • Strong hands-on experience using SAS to create CDISC-compliant outputs in a regulated clinical environment.
  • Solid understanding of SDTM, ADaM, and clinical data standards.
  • Experience in writing and validating dataset specifications.
  • Familiarity with P21 software.
  • Excellent written and verbal communication skills.

Preferred Qualifications

  • Experience with R and Python is a strong plus.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Strong attention to detail and problem-solving skills.