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Senior Clinical Sas Programmer Jobs (NOW HIRING)

We are looking for Clinical SAS Developer for our client in Upper Gwynedd, PA / Rahway, NJ . Job Title: Clinical SAS Developer Job Location: Upper Gwynedd, PA / Rahway, NJ Job Type: Contract Job ...

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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 ...

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 ...

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 ...

Senior SAS Programmer Location: Hybrid - Okemos, MI (Minimum 2 days onsite weekly; moving to 3 days/week soon) · We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work ...

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 ...

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Senior SAS Programmer

Winnetka, IL · Remote

$87K - $111K/yr

Brief Description The Senior SAS Programmer in the Biostatistics Department is responsible for: * Having the experience and expertise to handle complex research or development statistical programming ...

Senior SAS Programmer Location: Okemos, MI (Minimum 3 days onsite weekly) Duration: Long term Rate: Market f2f is must Responsibilities: · Participates in requirements and design sessions, then ...

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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Senior Clinical Sas Programmer information

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How much do senior clinical sas programmer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for senior clinical sas programmer in the United States is $54.05, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $61.30 per hour, depending on experience, location, and employer.

What are some typical challenges faced by Senior Clinical SAS Programmers when managing multiple clinical trial projects simultaneously?

Senior Clinical SAS Programmers often juggle multiple projects at various stages, which can present challenges such as prioritizing tasks, meeting tight regulatory deadlines, and ensuring data quality across studies. Effective communication and collaboration with statisticians, data managers, and clinical teams are essential to address emerging issues quickly. Familiarity with regulatory submission standards and proven organizational skills help in managing the workflow and maintaining consistency in deliverables.

What is a Senior Clinical SAS Programmer?

A Senior Clinical SAS Programmer is a specialized professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in pharmaceutical, biotechnology, or contract research organizations. They are responsible for developing, validating, and maintaining programs that transform raw clinical data into statistical tables, listings, and figures (TLFs) for regulatory submissions and study reports. In addition to technical programming tasks, senior SAS programmers often review code from junior programmers, ensure compliance with regulatory standards, and collaborate with statisticians, data managers, and clinical teams. Their expertise is critical for ensuring data integrity and supporting the success of clinical research projects.

What are the key skills and qualifications needed to thrive as a Senior Clinical SAS Programmer, and why are they important?

To thrive as a Senior Clinical SAS Programmer, you need advanced proficiency in SAS programming, a solid understanding of clinical trial data, and typically a degree in statistics, computer science, or a related field. Expertise in CDISC standards (SDTM, ADaM), experience with clinical data management systems, and familiarity with regulatory submission requirements are essential technical qualifications. Strong analytical thinking, attention to detail, and effective communication skills help in collaborating with cross-functional teams and ensuring data quality. These skills ensure accurate data analysis, compliance with regulatory standards, and successful support of clinical research objectives.
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Infographic showing various Senior Clinical Sas Programmer job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, 12% Part Time, and 12% Contract. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $112,418 per year, or $54 per hour.

Clinical SAS Programmer

Interon IT Solutions

Chantilly, VA • Remote

Contractor

Posted 4 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.