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Sas Programmer Oncology Jobs (NOW HIRING)

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and ... Experience supporting immunology, respiratory or oncology studies would be a plus. * Excellent ...

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Sas Programmer Oncology information

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$14

$49

$79

How much do sas programmer oncology jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for sas programmer oncology in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

What is the difference between Sas Programmer Oncology vs SAS Data Analyst?

AspectSas Programmer OncologySAS Data Analyst
Required CredentialsBachelor's in Computer Science, Biostatistics, or related field; SAS certification often preferredBachelor's in Statistics, Data Science, or related; SAS certification beneficial
Work EnvironmentPharmaceutical or healthcare research settings, clinical trial data managementVarious industries including healthcare, finance, and marketing; data analysis roles
Employer & Industry UsagePharmaceutical companies, clinical research organizations, healthcare institutionsCorporations, consulting firms, healthcare organizations, government agencies

While both roles involve SAS programming skills, Sas Programmer Oncology specializes in clinical trial data within the oncology field, focusing on pharmaceutical research. SAS Data Analysts have broader data analysis responsibilities across multiple industries. The key differences lie in industry focus, specific domain knowledge, and the type of data handled.

What are the key skills and qualifications needed to thrive as a SAS Programmer in Oncology, and why are they important?

To thrive as a SAS Programmer in Oncology, you need expertise in statistical programming, clinical data analysis, and a solid understanding of oncology clinical trial processes, typically supported by a degree in a quantitative field. Proficiency in SAS software, CDISC standards (such as SDTM and ADaM), and familiarity with clinical trial databases and regulatory submission requirements are essential. Strong attention to detail, problem-solving skills, and effective communication are crucial soft skills for ensuring data accuracy and collaborating with cross-functional teams. These skills and qualifications are vital to delivering reliable analyses that support regulatory approvals and advance oncology research.

What are SAS Programmers in Oncology?

SAS Programmers in oncology are specialized professionals who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data related to cancer research and treatment. They work closely with statisticians, clinical data managers, and other stakeholders to ensure accurate data analysis and regulatory compliance. Their responsibilities include creating datasets, performing statistical analyses, generating tables, listings, and figures (TLFs), and ensuring data integrity for oncology clinical trials. This role is crucial for supporting drug development and approval processes in oncology.

How does an SAS Programmer in oncology typically collaborate with clinical research teams?

As an SAS Programmer in oncology, you will work closely with clinical data managers, statisticians, and medical writers to ensure the accuracy and integrity of clinical trial data. Collaboration often involves participating in regular project meetings, clarifying data requirements, and providing statistical outputs for interim and final study reports. You may also help troubleshoot data discrepancies and contribute to process improvements, making strong communication and teamwork skills essential in this role.
More about Sas Programmer Oncology jobs
Infographic showing various Sas Programmer Oncology job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 2% As Needed, 81% Full Time, 8% Part Time, and 8% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.
Senior SAS Programmer

Senior SAS Programmer

Integrated Resources INC

Woodcliff Lake, NJ โ€ข On-site

Contractor

Posted 21 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