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Senior Statistical Programmer Jobs in Ohio (NOW HIRING)

Guidehouse

Biostatistician Lead

Beavercreek, OH

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This individual will serve as the senior statistical authority responsible for ensuring ... Experience in statistical programming using SAS and at least one additional statistical language ...

SIERTEK

Senior Analyst*

Dayton, OH · On-site

$82K - $108K/yr

COM/CAREERS Position Overview Section The Senior Analyst provides advanced statistical ... Statistical Programming * Develop statistical programs and perform data analysis using: * SAS * SAS ...

SIERTEK LTD

Senior Analyst* (26.23)

Dayton, OH · On-site

$83K - $110K/yr

SierTeK Ltd. is seeking a Senior Analyst (Epidemiologist/Statistician/Mathematician) to support an ... Statistical Programming * Develop statistical programs and perform data analysis using: * SAS * SAS ...

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Senior Statistical Programmer information

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How much do senior statistical programmer jobs pay per year?

As of Aug 16, 2026, the average yearly pay for senior statistical programmer in Ohio is $121,968.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,700.00 and $140,700.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the key skills and qualifications needed to thrive as a senior statistical programmer, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What are the most commonly searched types of Statistical Programmer jobs in Ohio?

The most popular types of Statistical Programmer jobs in Ohio are:

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Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in Ohio as of August 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 70% In-person, and 30% Remote job distribution, with an average salary of $121,968 per year, or $58.6 per hour.

Principal Statistical Programmer

Neshent Technologies

Kenwood, OH • On-site

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.

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