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How much do clinical sas programmer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical sas programmer in Ohio is $51.37, according to ZipRecruiter salary data. Most workers in this role earn between $39.52 and $64.66 per hour, depending on experience, location, and employer.

What is a clinical SAS programmer?

A Clinical SAS Programmer is a professional who uses SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and medical research industries. Their main responsibilities include creating programs to clean, organize, and analyze clinical data, generating summary tables and listings, and ensuring the accuracy and compliance of data for regulatory submissions. They work closely with biostatisticians, data managers, and clinical researchers to support drug development and approval processes.

What is a SAS clinical programmer?

As a SAS clinical programmer, your primary responsibilities are the management and analysis of large datasets of information from clinical trials. Your job duties include using and programming the statistical analysis system, or SAS software suite, to develop tables and reports about the interdependencies of data points and the efficacy of trial-phase clinical therapies. The qualifications for a career as a SAS clinical programmer are a bachelor’s degree in statistics or computer science and experience in the pharmaceutical or clinical industries. You must develop strong SAS technical skills and problem-solving skills to succeed in a career as a SAS clinical programmer.

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 strong programming skills in SAS, a solid understanding of clinical trial data, and often a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (SDTM, ADaM), clinical data management systems, and regulatory submission processes is typically required. Attention to detail, problem-solving abilities, and effective communication skills help you collaborate with cross-functional teams and ensure data quality. These skills are vital for ensuring accurate data analysis and compliance with industry regulations in clinical research.

What are 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, ensuring data integrity, and adhering to strict regulatory guidelines. They must also collaborate closely with biostatisticians and data managers to resolve data discrepancies and interpret study protocols accurately. Timely delivery of high-quality statistical outputs, such as tables, listings, and figures, is critical, often under tight deadlines. Effective communication and attention to detail are essential to overcome these challenges and deliver reliable results.

What is the difference between Clinical Sas Programmer vs Clinical Data Analyst?

AspectClinical Sas ProgrammerClinical Data Analyst
Required CredentialsBachelor's in IT, Life Sciences, or related; SAS certification often preferredBachelor's in Statistics, Data Science, or related; often requires statistical or data analysis certifications
Work EnvironmentPharmaceutical or CRO settings, working with SAS software to develop datasets and reportsResearch or clinical settings, analyzing clinical data to generate insights and reports
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, research organizations, healthcare providers

While both roles involve working with clinical data, Clinical Sas Programmers focus on programming, data manipulation, and report generation using SAS software. Clinical Data Analysts primarily analyze data to interpret results and support decision-making. Both roles require strong analytical skills but differ in their core responsibilities and technical focus.

Are Clinical SAS Programmers in demand?

Clinical SAS Programmers are in high demand due to the ongoing need for data analysis and reporting in clinical trials. Skills in SAS programming, knowledge of regulatory requirements, and experience with electronic data capture systems increase employability in this field.

Is a clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the pharmaceutical and healthcare industries, focusing on data analysis and reporting using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience in clinical trial processes. The role typically requires strong analytical skills and knowledge of regulatory standards such as GCP and FDA guidelines.

What is the salary of clinical SAS programmer?

The salary of a clinical SAS programmer typically ranges from $70,000 to $110,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced programmers with advanced skills can earn higher salaries, especially in competitive markets or with specialized knowledge of clinical trial data analysis.
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Clinical Sas Programmer jobs near you
Infographic showing various Clinical Sas Programmer job openings in Ohio as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $106,857 per year, or $51.4 per hour.

SAS Programmer - Entry Level

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 28 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 74 rated research

Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry level 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
  • BS in Statistics, Mathematics, Life Sciences, or related field
  • SAS Programming experience required
  • Minimum 3.4 GPA 
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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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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