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Pharmaceutical Sas Programmer Jobs (NOW HIRING)

SPECTRAFORCE

SAS Programmer

North Chicago, IL · On-site

Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...

Collabera

SAS Programmer

Jersey City, NJ · On-site

The role of the Senior Statistical Programmer is to perform statistical programming activities for ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...

Spectra force

SAS Programmer

North Chicago, IL · On-site

Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...

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How much do pharmaceutical sas programmer jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for pharmaceutical sas programmer in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a pharmaceutical SAS programmer?

To thrive as a Pharmaceutical Sas Programmer, you need strong expertise in SAS programming, clinical data analysis, and a solid understanding of regulatory requirements, typically supported by a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (such as SDTM and ADaM), exposure to clinical trial management systems, and SAS certifications are commonly expected. Attention to detail, problem-solving abilities, and effective communication skills help distinguish top performers in this role. These skills are essential for ensuring the accuracy, compliance, and clarity of clinical trial data submitted to regulatory authorities.

What is a pharmaceutical SAS programmer?

A Pharmaceutical SAS Programmer is responsible for analyzing clinical trial data using SAS software. They develop, validate, and manage programs to generate statistical outputs like tables, listings, and figures for regulatory submissions. Their role ensures compliance with industry standards such as CDISC (SDTM and ADaM) and FDA guidelines. They collaborate with statisticians, data managers, and regulatory teams to ensure accurate data reporting and support drug development processes.

What types of projects or responsibilities can I expect as a pharmaceutical SAS programmer?

As a Pharmaceutical Sas Programmer, you will primarily be tasked with writing and validating programs to analyze clinical trial data, generate tables, listings, and figures (TLFs), and ensure outputs meet regulatory standards. You may collaborate closely with biostatisticians, clinical data managers, and other programmers to interpret datasets, implement statistical analysis plans, and troubleshoot issues in data processing. The work is typically project-based, often requiring you to prioritize multiple studies or phases simultaneously and adhere to tight deadlines. This role offers exposure to the full drug development lifecycle and provides valuable experience for advancing into senior programming, data management, or biostatistics positions.

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Pharmaceutical Sas Programmer jobs near you
Infographic showing various Pharmaceutical Sas Programmer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

SAS Programmer

Oasis Technology Inc.

East Brunswick, NJ • On-site

Contractor

Re-posted 8 days ago

Job description

Job Description
  • Minimum of 3 years of experience defining SAS analysis requirements and performing SAS programming
  • BASE SAS Cert
  • Expert knowledge of base SAS and SAS Macros for SAS software development
  • Design, development and unit-testing od SAS program code, functions and scripts to efficiently extract, merge and manipulate data
  • Expert Knowledge of lookup tables for SAS for SAS software development
  • Expert knowledge in proposing and implementing improvements/efficiencies for SAS software development to create repeatable business processes for use by others
  • Excellent oral and written communication skills in English
  • Experience clarifying business and technical requirements with data requestors
  • Provides technical and analytic input to peer review team
Qualifications
  • BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.
  • Must Provide Three Professional Reference including their official email address at the time of application.
  • Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.
Additional Information

Visa Status

  • Only US Citizens, Green Card, EAD and OPT holders.
  • No H1B Holders and Third-Parties.
  • No Corp-Corp

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