ZipRecruiter

Log In

1

Sas Programmers Jobs in Ohio (NOW HIRING)

Huntington Bank

SAS Viya Developer/Admin

Columbus, OH · On-site

$70K - $140K/yr

As an SAS Viya Developer/Admin for AML Software and systems, you will install, configure vendor software, applications, and data ingestion frameworks, which are typically complex in nature, or ...

New

Huntington

SAS Viya Developer/Admin

Columbus, OH · On-site

$70K - $140K/yr

As an SAS Viya Developer/Admin for AML Software and systems, you will install, configure vendor software, applications, and data ingestion frameworks, which are typically complex in nature, or ...

Huntington

SAS Viya Developer/Admin

Columbus, OH

$70K - $140K/yr

As an SAS Viya Developer/Admin for AML Software and systems, you will install, configure vendor software, applications, and data ingestion frameworks, which are typically complex in nature, or ...

previous page

Showing results 41-60

All JobsSas Programmers JobsSas Programmers Jobs in Ohio

Sas Programmers information

See Ohio salary details

$13

$46

$75

How much do sas programmers jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for sas programmers in Ohio is $46.59, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $58.51 per hour, depending on experience, location, and employer.

What is the difference between Sas Programmers vs Data Analysts?

AspectSas ProgrammersData Analysts
Required CredentialsProficiency in SAS, often with a degree in computer science, statistics, or related fieldsOften have degrees in statistics, mathematics, or data science; may also use SAS but focus more on analysis
Work EnvironmentTypically work in IT or analytics teams within industries like healthcare, finance, or governmentWork across various industries, focusing on interpreting data and generating reports
Employer & Industry UsageUsed mainly in industries with legacy systems or regulatory requirements requiring SASWidely used across industries for data interpretation and business insights

While both roles involve working with data, Sas Programmers primarily focus on developing and maintaining SAS-based data processing and reporting systems, whereas Data Analysts concentrate on interpreting data to provide actionable insights. The roles often overlap, but Sas Programmers are more technical and coding-focused, while Data Analysts emphasize analysis and visualization.

Can you work remotely as a SAS programmer?

Many SAS programmers can work remotely, especially with the increasing adoption of telecommuting in data analysis and programming roles. Remote work often requires strong communication skills, proficiency with SAS software, and sometimes specific certifications or security clearances depending on the employer. Flexibility varies by company and project requirements.

Are SAS programmers in demand?

SAS programmers are in demand in industries such as healthcare, finance, and pharmaceuticals that rely on data analysis and reporting. The role requires proficiency in SAS software, data management, and statistical analysis, with job growth driven by increasing data-driven decision making across sectors.

What are popular job titles related to Sas Programmers jobs in Ohio?

For Sas Programmers jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Sas Programmers jobs in Ohio look for?

The top searched job categories for Sas Programmers jobs in Ohio are:

Sas Programmers jobs near you
Infographic showing various Sas Programmers job openings in Ohio as of August 2026, with employment types broken down into 51% Full Time, 47% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $96,903 per year, or $46.6 per hour.

Principal Statistical Programmer

Neshent Technologies

Cincinnati, OH

Full-time

Posted 17 days ago

Job description

We are seeking an experienced Principal Statistical Programmer to lead statistical programming activities for clinical development programs. The ideal candidate will have strong expertise in SAS programming, CDISC standards, ADaM datasets, TLF development, regulatory submissions, and clinical trial data analysis. This role will provide technical leadership, mentor statistical programmers, and collaborate with cross-functional clinical teams.

Required Skills & Experience
  • Experience leading a team of statistical programmers supporting clinical development programs.
  • Strong proficiency in SAS programming for developing and validating:
    • ADaM datasets
    • Tables, Listings, and Figures (TLFs)
    • Statistical analyses
  • Good knowledge of R programming and other statistical programming languages preferred.
  • Strong understanding of SAS programming concepts and the clinical study lifecycle.
  • In-depth knowledge of CDISC standards (SDTM/ADaM) and regulatory requirements.
  • Experience supporting regulatory filings and submission documentation.
  • Experience working in therapeutic areas such as Oncology, Immunology, Neuroscience, or similar domains.
  • Strong communication and collaboration skills with cross-functional teams.
  • Ability to estimate project programming efforts and manage competing priorities.
Roles and Responsibilities
  • Lead statistical programming activities for assigned compounds, indications, or therapeutic areas.
  • Manage and mentor statistical programmers, analysts, and senior analysts.
  • Plan resources, track deliverables, and ensure timely completion of programming activities.
  • Develop and oversee SAS programs for ADaM dataset creation following CDISC standards.
  • Develop and review SAS programs for Tables, Listings, and Figures (TLFs).
  • Ensure consistency and quality of ADaM datasets across individual studies and integrated analyses.
  • Support regulatory submissions by preparing documentation such as reviewer guides and data definition documents.
  • Develop standard SAS macros, programming standards, and operating procedures.
  • Ensure compliance with quality processes and clinical programming best practices.
  • Collaborate with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams.
Preferred Qualifications
  • Experience in pharmaceutical, biotechnology, or clinical research environments.
  • Strong knowledge of clinical trial programming and regulatory submission processes.
  • Excellent leadership, problem-solving, and organizational skills.
  • Ability to work effectively in a dynamic, deadline-driven environment.

Apply