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Pharmaceutical Sas Programmer Jobs (NOW HIRING)

Navitas Life Sciences

Senior Statistical Programmer

Background in statistics and statistical analysis is desirable * 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming * Strong competence in SAS ...

Crowdstaffing

Biostatistician

Emeryville, CA · On-site

PHARMACEUTICAL FDA * SAS * STATISTICAL ANALYSIS * BIOSTATISTICS * Minimum 2 years experience in ... Skilled SAS programming knowledge. * Demonstration of innovation by development or novel ...

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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.
SAS Programmer - Advanced Degrees

SAS Programmer - Advanced Degrees

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, PTO

Posted 27 days ago

Medpace rating

8.4

Company rating: 8.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

15th of 57 rated research

Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Write SAS programs for use in creating analysis datasets, tables, listings, and figures
  • Using SAS, program, validate and maintain mapped database
  • Program edit checks for external data
  • Coordinate communication and issues with Data Management regarding database specifications and data transfers
Qualifications
  • MS in Mathematics, Data Science, or related field
  • SAS Base Certification required;
  • Minimum 3.4 GPA 
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

  • Cincinnati Campus Overview
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Employment Type: OTHER
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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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