ZipRecruiter

Log In

1

Clinical Sas Jobs (NOW HIRING)

CICONIX, LLC

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

SPECTRAFORCE

SAS Programmer

North Chicago, IL

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 ...

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 ...

Collabera

SAS Programmer

Jersey City, NJ · On-site

This position performs statistical programming for clinical studies, integrated summaries, and in ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...

previous page

Showing results 41-60

All JobsClinical Sas Jobs

Clinical Sas information

See salary details

$19

$54

$80

How much do clinical sas jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical sas in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What are some 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 from multiple sources, ensuring strict compliance with regulatory standards (like CDISC, SDTM, and ADaM), and meeting tight project deadlines. They must also collaborate closely with biostatisticians, data managers, and clinical teams to ensure data accuracy and consistency. Staying updated with evolving industry standards and software updates is crucial, as is maintaining clear documentation to support regulatory submissions.

What is the difference between Clinical Sas vs Clinical Data Manager?

AspectClinical SasClinical Data Manager
Required CredentialsBiostatistics, SAS certification, or related trainingBiostatistics, data management certifications, or related degrees
Work EnvironmentStatistical analysis, programming, and reporting in clinical trialsData collection, validation, and database management in clinical studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research organizations

Clinical Sas professionals focus on statistical analysis and programming using SAS software to interpret clinical trial data. In contrast, Clinical Data Managers oversee data collection, validation, and database management to ensure data quality. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

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

To thrive as a Clinical SAS Programmer, you need expertise in SAS programming, a solid understanding of clinical trial data, and a degree in life sciences, statistics, or a related field. Familiarity with CDISC standards (SDTM/ADaM), clinical data management systems, and regulatory submission requirements is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills ensure accurate data analysis and reporting, which are critical for regulatory compliance and successful clinical trial outcomes.

What is a clinical SAS?

Clinical SAS professionals are specialists who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. They play a critical role in ensuring data integrity and compliance with regulatory standards by generating statistical reports, tables, listings, and graphs for clinical studies. These professionals often collaborate with biostatisticians, clinical researchers, and data managers to support the drug development and approval process.
More about Clinical Sas jobs

What cities are hiring for Clinical Sas jobs?

Cities with the most Clinical Sas job openings:

What states have the most Clinical Sas jobs?

States with the most job openings for Clinical Sas jobs include:

What job categories do people searching Clinical Sas jobs look for?

The top searched job categories for Clinical Sas jobs are:

Clinical Sas jobs near you
Infographic showing various Clinical Sas job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

SAS Programmer - Advanced Degrees

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 27 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 73 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) 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

Medpace logo

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

View All Medpace Jobs

Apply