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Clinical Sas Programer Jobs (NOW HIRING)

HCLTech

SAS Developer

North Wales, PA

Extensive programming experience in a clinical trial environment (CRO/Pharma). Expertise in SAS ... BASE, SAS/STAT, and SAS/MACRO. In-depth knowledge of CDISC standards and regulatory submission ...

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 ...

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 ...

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 ...

SPECTRAFORCE

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

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 ...

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Clinical Sas Programer information

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How much do clinical sas programer jobs pay per hour?

As of Jun 13, 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
Infographic showing various Clinical Sas Programer job openings in the United States as of June 2026, with employment types broken down into 2% Locum Tenens, 65% Part Time, 32% Contract, and 1% Nights. Highlights an 100% Hybrid job distribution, with an average salary of $112,399 per year, or $54 per hour.
Sr, SAS Programming Analyst

Sr, SAS Programming Analyst

Integrated Resources INC

Woodcliff Lake, NJ

Contractor

Posted 28 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Sr SAS Programmer Analyst - SDTM

  • Responsible for SDTM data creation and delivery for oncology studies.
  • Prepare SDTM Mapping specification following company standards.
  • Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials.
  • Develop programs to create SDTM datasets and Define.xml for statistical analysis, tables & listings, and regulatory submissions.
  • Perform Open CDISC validation, coordinate to resolve issues, prepare associated documentation
  • Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.
  • Ensure all programming activities and processes performed are conducted according to standard operating procedures, good programming practices, and GCP guidelines. 
  • Strong problem-solving skills;
  • Able to work independently and as a team player; Good organizational, time management, and project management skills ;
  • Capable of communicating technical concepts
  • Good understanding of system development life cycles, GCP, and related Regulatory guidelines.
  • Should be able to manage the assigned projects independently with minimum supervision.
Qualifications
  • BS or MS in Computer Science or related field;
  • 5-7 years of strong experience in programming with clinical trial data and developing programs, testing, and documentation;
  • Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SQL;
  • Extensive experience of handling SDTM mapping, related data structures, and programming to create SDTM data sets;
  • Extensive experience in SDTM validation using OpenCDisc.
  • Good knowledge in developing Define.xml and its validation.
  • Extensive experience of handling external data, e.g., laboratory data, PK, ECG, Biomarker, Imaging, etc.
  • Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG;
  • Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus;
  • Knowledge of using JReview/IReview is a plus;
Additional Information

Best Regards

Mohit Garg

Integrated resources Inc | Team Recruitment | 732-429-1634


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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