ZipRecruiter

Log In

1

Clinical Sas Programer Jobs (NOW HIRING)

E-Solutions

SDTM/Clinical SAS

Rahway, NJ · On-site

1.Must have 6+ yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS ... Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer ...

VENESCO LLC

SAS Programmer

Falls Church, VA · On-site

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements: Key Responsibilities: • Develop SAS programs for tables, listings ...

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: Develop SAS programs for tables, listings, and ...

Venesco LLC

SAS Programmer

Falls Church, VA · On-site

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: • Develop SAS programs for tables, listings ...

Venesco

SAS Programmer

Falls Church, VA · On-site

Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements Key Responsibilities: • Develop SAS programs for tables, listings ...

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical development services. They are seeking an Entry Level SAS Programmer to join their Biostatistics ...

Medpace

SAS Programmer - Experienced

Cincinnati, OH · On-site

Medpace is a full-service clinical contract research organization (CRO) that provides clinical ... They are currently seeking an experienced SAS Programmer to join their Biostatistics team to write ...

Integrated Resources INC

SAS Programming

Madison, NJ · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Performs all SAS programming required for clinical trial analysis and reporting; Ensures that activities and ...

Medpace

SAS Programmer - Experienced

Cincinnati, OH · On-site

Biostatistics Team Sas Programmer Our corporate activities are growing rapidly, and we are ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

next page

Showing results 1-20

All JobsClinical Sas Programer Jobs

Clinical Sas Programer information

See salary details

$19

$54

$80

How much do clinical sas programer jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for clinical sas programer 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 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 good understanding of clinical trial data, and usually a degree in life sciences, statistics, or a related field. Familiarity with CDISC standards (SDTM/ADaM), clinical data management systems, and often certifications like Base SAS are highly valued. Attention to detail, problem-solving abilities, and effective communication are essential soft skills for this role. These competencies ensure accurate statistical analysis and regulatory compliance, which are critical for successful clinical research outcomes.

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 and biotechnology industries. They are responsible for programming datasets, generating tables, listings, and figures, and ensuring data accuracy and compliance with regulatory standards. Clinical SAS Programmers work closely with biostatisticians, data managers, and clinical researchers to support the statistical analysis and reporting needs of clinical studies.

How do Clinical SAS Programmers typically collaborate with clinical data managers and statisticians during a clinical trial?

Clinical SAS Programmers work closely with clinical data managers and statisticians throughout the lifecycle of a clinical trial. They are responsible for programming datasets, validating data, and generating analysis outputs like tables, listings, and figures. Effective collaboration ensures that data standards are met, timelines are adhered to, and the statistical analysis plan is correctly implemented. Regular meetings and clear communication channels help resolve data discrepancies and facilitate smooth workflow between teams.

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

AspectClinical SAS ProgrammerClinical Data Analyst
Required CredentialsBachelor's in IT, Statistics, or related field; SAS certification often preferredBachelor's in Statistics, Data Science, or related field; often requires knowledge of data analysis tools
Work EnvironmentPharmaceutical or biotech companies, CROs, clinical research settingsHealthcare organizations, research institutions, pharmaceutical companies
Employer & Industry UsagePrimarily in clinical trial data management and reportingData interpretation, reporting, and insights in clinical and healthcare settings

While both roles involve working with clinical data, Clinical SAS Programmers focus on programming and data management using SAS software, whereas Clinical Data Analysts interpret data and generate reports. The roles often overlap but serve different primary functions within clinical research teams.

More about Clinical Sas Programer jobs
What job categories do people searching Clinical Sas Programer jobs look for? The top searched job categories for Clinical Sas Programer jobs are:
Clinical Sas Programer jobs near you
SDTM/Clinical SAS

SDTM/Clinical SAS

E-Solutions

Rahway, NJ • On-site

Other

Posted 11 days ago

Job description

1.Must have 6+ yrs of exp in clinical domain
2.Strong knowledge of SDTM
3.Create advanced SAS macros, templates, and utilities for efficient data processing
4.Act as the primary programming point of contact for biostatisticians and study teams
5.Perform peer review of code and documentation for accuracy and traceability
6.Review CRF (Case Report Form) annotations and data specifications.
7.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines
Skill:
1.Extensive programming experience in a clinical trial environment (CRO/Pharma).
2.Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
3.In-depth knowledge of CDISC standards and regulatory submission requirements

Apply