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Clinical Sas Programer Jobs (NOW HIRING)

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

Entry Level SAS Programmer Our corporate activities are growing rapidly, and we are currently ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

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 ...

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 ...

Diverse Lynx

SAS Viya developer

Raleigh, NC · On-site

The ideal candidate will lead end-to-end clinical data workflows, regulatory submissions, and ... SAS/Python/R programming, combined with experience in cloud platforms (AWS/Azure) and clinical data ...

InterSources

SAS / Statistical Programmer

Chicago, IL · On-site

Clinical Trial Programmer Major tasks of position: Understanding of clinical trial objectives ... Develop programs that convert raw SAS datasets into standard format and improve existing programs ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Knowledge of R programming in clinical trials Familiarity of the drug development process. Knowledge of CDISC standards and electronic submission requirements. Strong SAS and SAS Macro language ...

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 ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA · On-site

$145K - $156K/yr

Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS). * Comprehensive understanding of clinical trial processes, data flow, and clinical trial data ...

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 ...

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Clinical Sas Programer information

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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.

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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
SAS Programmer III

SAS Programmer III

Katalyst HealthCares & Life Sciences

Durham, NC • On-site

Other

Posted 18 days ago

Job description

Job Title

Responsibilities:

  • Review and ensure accurate and high-quality statistical programming deliverables from CRO.
  • Perform generation, validation and QC/QA of SDTM, ADaM and TFL output in accordance with SOPs, SOIs, and guidance documents.
  • Create and maintain specifications as per SDTM/ADaM standard and study SAP.
  • Define and create ad-hoc reports and listings for clinical teams.
  • Develop, implement and maintain SAS programming standards.
  • Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as necessary.
  • Verifies completeness of relevant study deliverables prior to release from the group Maintains all required study documentation.
  • Consults and provides input into system validation efforts including tool maintenance activities.
  • Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.
  • Work in tandem with Biostatistics and Data Management member on various clinical projects.
  • Review CRF annotations and data specifications.
  • Perform quality control on final reports.
  • Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
  • Perform clinical study report and/or exploratory analysis for oncology clinical study
  • Perform validation of ADaM datasets and TLFs per SAP.
  • Effectively review and comment on vendor programming deliverables and help resolve technical difficulties.

Requirements:

  • BS or above in computer science/statistics with at least 5 years of SAS experience in major pharma or CRO.
  • Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis
  • Proficient computer skills across multiple applications and OS environments
Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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