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Clinical Sas Jobs (NOW HIRING)

Yochana

Clinical SAS Developer:

Passaic, NJ · On-site

Job Title Must have 6-8 yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point ...

Omni Inclusive

SAS Clinical Developer

Rahway, NJ · On-site

SDTM/Clinical SAS 1. Must have 6-8 years of experience in the clinical domain 2. Strong knowledge of SDTM 3. Create advanced SAS macros, templates, and utilities for efficient data processing 4. Act ...

E-Solutions

SDTM/Clinical SAS

Rahway, NJ · On-site

Must have 6+ yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the primary programming point of ...

Cynet Systems

Clinical SAS Developer

North Wales, PA · On-site

$43 - $48/hr

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 ...

CYNET SYSTEMS

Clinical SAS Developer

Upper Gwynedd, PA · On-site

$43 - $48/hr

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 ...

Omni Inclusive

SAS programmers

Rahway, NJ · On-site

Looking for 10+ years of clinical SAS programmers having in depth knowledge of CDISC SDTM. Gathering data from all available source and using SAS to process it. Creating and writing programs.

Omni Inclusive

SDTM Programmer (SDTM, SAS)

Rahway, NJ · On-site

Job Title Looking for 5+ years of clinical SAS programmers having in depth knowledge of CDISC SDTM Gathering data from all available source and using SAS to process it. Creating and writing programs ...

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Clinical Sas information

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$19

$54

$80

How much do clinical sas jobs pay per hour?

As of Jul 4, 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 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, 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.
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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 60% As Needed, 20% Full Time, and 20% Part Time. Highlights an 93% Physical, 2% Hybrid, and 5% 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 25 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.