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Pharmaceutical Sas Programmer Jobs (NOW HIRING)

MMS

Senior Statistical Programmer - Remote

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Advanced user in SAS programming, SAS Base, and SAS Macros. * Advanced knowledge of E-Submission ...

EDETEK

Senior Statistical Programmer

Minimum of 5 years of experience in statistical programming within the pharmaceutical or clinical research industry. * Proficiency in SAS programming; experience with R and other statistical software ...

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How much do pharmaceutical sas programmer jobs pay per hour?

As of Jun 17, 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 in the Pharmaceutical Sas Programmer position, and why are they important?

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 job?

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 June 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% 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.

Senior Statistical Programmer - Remote

MMS

Canton, MI • On-site

Full-time

Posted 16 days ago

Job description

About MMS
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Applicants must be legally authorized to work in the U.S. for any employer; we cannot sponsor visas (e.g., H-1B) or offer work authorization transfers at this time.
Job Specific Skills:
  • Mastery and trained on generating tables, listings, and graphs from clinical trial databases using SAS.
  • Utilizes System Development Life Cycle (SDLC) for programming deliverables.
  • Advanced user in SAS programming, SAS Base, and SAS Macros.
  • Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
  • Mastery and trained on SDTM standards including ability to write specifications.
  • Advanced knowledge of ADaM standards including supporting specification writing.
  • Proficient with MS Office applications.
  • Advanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements.
  • Advanced experience with pooling of data sets for submissions.
  • Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
  • Lead study or small programming project teams.
Job Requirements:
  • Masters required for all Statistics roles.
  • Minimum of 5 years’ experience in Statistical Programming or similar field required.
  • Expert knowledge of scientific principles and concepts. 
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications. 
  • Hands-on experience with clinical trial and pharmaceutical development preferred.   
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems. 
  • Excellent problem-solving skills. 
  • Good organizational and communication skills. 
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.  
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.  

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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