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Junior Sas Programmer Jobs (NOW HIRING)

... SAS, Python, computer vision, data visualization tools Excellent written and verbal communication ... computer engineering, electrical engineering, information systems, IT Highly motivated, self ...

As an SAS Viya Developer/Admin for AML Software and systems, you will install, configure vendor ... Provide technical guidance and training to junior resources * Perform other duties as assigned ...

As an SAS Viya Developer/Admin for AML Software and systems, you will install, configure vendor ... Provide technical guidance and training to junior resources * Perform other duties as assigned ...

Who Should Apply Recent Computer science/Engineering /Mathematics/Statistics or Science Graduates ... NLP, Text mining, Tableau, PowerBI, SAS, Tensorflow If you get emails from our skill enhancement ...

Knowledge of Statistics, SAS, Python, Computer Vision, data visualization tools * Excellent written ... it's a junior or entry-level position. The additional skills and project work with hands-on ...

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Junior Sas Programmer information

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How much do junior sas programmer jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for junior sas programmer in the United States is $26.96, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $33.17 per hour, depending on experience, location, and employer.

What are the typical responsibilities of a Junior SAS Programmer on a daily basis?

As a Junior SAS Programmer, your main responsibilities usually include writing and maintaining SAS code to clean, validate, and analyze data sets, often under the guidance of more senior team members. You'll assist in generating reports, documenting programming processes, and participating in team meetings to discuss project progress or troubleshoot issues. Collaboration with data analysts, statisticians, and project managers is common, as is adapting to new datasets and receiving feedback to refine your work. This role offers valuable hands-on experience and is a great foundation for advancing into senior programming or data analyst positions.

What is a Junior SAS Programmer job?

A Junior SAS Programmer is an entry-level role responsible for writing and debugging SAS code to manage, analyze, and report data, often in industries like healthcare, finance, or research. They assist in data cleaning, validation, and generating reports based on client or business needs. Typically, they work under the supervision of senior programmers or statisticians and collaborate with data analysts or researchers. Strong knowledge of SAS programming, SQL, and data manipulation techniques is essential for this role.

What are the key skills and qualifications needed to thrive in the Junior Sas Programmer position, and why are they important?

To thrive as a Junior SAS Programmer, you need a basic understanding of SAS programming, statistics, and data management, typically supported by a degree in computer science, mathematics, or a related field. Familiarity with the SAS software suite, as well as knowledge of SQL and industry-relevant certifications, are commonly required. Problem-solving abilities, attention to detail, and effective communication help junior programmers excel within team settings. These skills ensure accurate data analysis, efficient code development, and clear collaboration with colleagues and stakeholders.

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What cities are hiring for Junior Sas Programmer jobs? Cities with the most Junior Sas Programmer job openings:
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Infographic showing various Junior Sas Programmer job openings in the United States as of June 2026, with employment types broken down into 2% Internship, 48% Full Time, 46% Part Time, 2% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $56,068 per year, or $27 per hour.

Other

Posted 12 days ago


Job description

Responsibilities:
  • Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
  • Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
  • Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
  • ssist in establishing standardized programming procedures and work instructions.
  • Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
  • Develop and maintain clinical processing workflow systems.
  • ssist in the development of client proposal documents.
  • Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
  • Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
  • Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
  • Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.) records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards).
  • ssist in updating/writing PROMETRIKA standard operating procedures (SOPs).
  • Develop tools in SAS® for data analysis and reporting that comply with regulatory requirements.
  • Develop specifications (e.g., metadata files), annotate CRFs and create SAS® programs for the mapping of raw datasets to CDISC SDTM standards.
  • Create define.xml files from metadata files for SDTM and ADaM.
  • Convert data received in other formats to SAS® datasets.
Requirements:
  • Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS.
  • Knowledge of SDTM, ADaM, FDA and ICH guidance.
  • Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
  • Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
  • Consistent experience as a lead statistical programmer on several concurrent projects.
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
  • Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
  • Excellent analytical skills.
  • Proven ability to learn new systems and function in an evolving technical environment.
  • bility to negotiate and influence to achieve results.
  • Good presentation skills.
  • Good business awareness/business development skills (including financial awareness).
  • bility to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Knowledge of other programming languages and database management software packages is a plus.