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Clinical Sas Programmer Jobs (NOW HIRING)

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 ...

If you have any other questions, please send me an email or call my direct line at 650-458-5456 SAS Developer Oakland, CA 6 months Contract Description Need to know programming in SAS and the SAS ...

Title: SAS Programmer Deliverables: * Prepare, update, and maintain all versions of statistical ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Job Title- SAS Programmer Location- Remote Duration- 12 Months (C2H Role) Good SAS/SQL Experience with recent healthcare experience. What are the top 5-10 responsibilities for this position (please ...

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 ...

Programmer SAS Location: Abbott Park, IL, 60064 Responsibilities: SAS developer with 10+ year experience in base SAS plus Proc SQL Experience in SDTM standards, familiar with latest guidance ...

Senior SAS Programmer Location: Hybrid - Okemos, MI (Minimum 2 days onsite weekly; moving to 3 days/week soon) · We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work ...

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 ...

Minimum three years' experience in BASE SAS products and procedures and one year experience in ... Experience with DB programming is a plus. Ability to work in a rapidly changing and fast-paced ...

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 Programmer information

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$19

$54

$80

How much do clinical sas programmer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical sas programmer 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 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.

What cities are hiring for Clinical Sas Programmer jobs?

Cities with the most Clinical Sas Programmer job openings:

What are the most commonly searched types of Clinical Sas Programmer jobs?

The most popular types of Clinical Sas Programmer jobs are:

What states have the most Clinical Sas Programmer jobs?

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

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

The top searched job categories for Clinical Sas Programmer jobs are:

Infographic showing various Clinical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% 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.

Senior SAS Programmer

Integrated Resources INC

Woodcliff Lake, NJ • On-site

Contractor

Re-posted 28 days ago


Job description

Company Description

At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective
All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in.

Job Description

Job Title: Sr. SAS Programmer Analyst

Duration: 1 year+

Location : Woodcliff Lake, NJ

JOB DESCRIPTION:

  • Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials.
  • Develop programs for patient profiles and ad hoc reports for data review to support the clinical teams for Oncology trials.
  • Program data edit checks as necessary to facilitate Data Management's data cleaning activities.
  • 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.
  • Develop and maintain the programs including testing and organizing the SAS datasets, SAS programs and related documentation.
  • Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming skills.
Qualifications

REQUIREMENTS:

  • Need someone with writing macro and generic program experience. Candidates must be capable of writing complex generic system related macros and have written any generic programs or macros during their work experience.
  • Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/ SQL.
  • 7-10 years of experience in programming with clinical trial data and preparing programming and test documentation.
  • Extensive experience of handling external data, such as lab data, PK, ECG, Tumor, etc.
  • Experience with JReview is a plus.
  • Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG.
  • Good understanding of relational databases such as ORACLE, Knowledge of the EDC system, InForm, and underlying data structure is a plus.
  • Knowledge of data management process, good understanding of data cleaning process.
  • Strong problem solving skills
  • Able to work independently and a team player, good organizational and time management skills.
  • Capable of communicating technical concepts
  • Good understanding of system development life cycles, GCP, and related regulatory guidelines.
Additional Information

Regards,

Pooja Mishra | Team Recruitment | Mindlance, Inc. |

W: 732-243-0715


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