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Senior Statistical Programmer Jobs in Ohio (NOW HIRING)

Fortrea

Principal Biostatistician - FSP

Toronto, OH · On-site +1

$115K - $130K/yr

... programming support to your multidisciplinary global project team. About the team You will be part ... Lead the development of complex Statistical Analysis Plans, perform senior review of statistical ...

Ipsen

Sr. Director, Biostatistics

London, OH

Title: Sr. Director, Biostatistics Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a ... and statistical programming. WHAT - Main Responsibilities & Technical Competencies * Work as ...

Ra

Marketing Analytics Manager

Cincinnati, OH

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Manager

Columbus, OH

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Manager

Cleveland, OH

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Axogen

Sr. Engineer, Manufacturing/Processing

Vandalia, OH

$97K - $126K/yr

Job Summary of the Sr. Engineer, Manufacturing/Processing The Sr. Manufacturing Process Engineer ... Using statistical methods to determine in-control/out-of-control * Developing and implementing ...

Axogen

Sr. Engineer, Manufacturing/Processing

Vandalia, OH

$97K - $126K/yr

Job Summary of the Sr. Engineer, Manufacturing/Processing The Sr. Manufacturing Process Engineer ... Using statistical methods to determine in-control/out-of-control * Developing and implementing ...

Axogen

Sr. Engineer, Manufacturing/Processing

Vandalia, OH

$97K - $126K/yr

Job Summary of the Sr. Engineer, Manufacturing/Processing The Sr. Manufacturing Process Engineer ... Using statistical methods to determine in-control/out-of-control * Developing and implementing ...

Axogen

Sr. Engineer, Manufacturing/Processing

Vandalia, OH · On-site

$97K - $126K/yr

Job Summary of the Sr. Engineer, Manufacturing/Processing The Sr. Manufacturing Process Engineer ... Using statistical methods to determine in-control/out-of-control * Developing and implementing ...

giftHEALTH Inc

Senior Data Engineer

Columbus, OH · On-site

$123K - $138K/yr

Bachelor's Degree in mathematics, statistics, computer science, or other quantitative field and relevant work experience as a Senior Data Engineer * Experience : 6+ years of experience as a Data ...

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Senior Statistical Programmer information

See Ohio salary details

$78.4K

$122K

$159.2K

How much do senior statistical programmer jobs pay per year?

As of Jun 26, 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 job?

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 in the Senior Statistical Programmer position, 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 June 2026, with employment types broken down into 95% Full Time, 3% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $121,968 per year, or $58.6 per hour.

Sr. Statistical Programmer

Katalyst Healthcares and Life Sciences

Cincinnati, OH • On-site

Other

Posted 3 days ago

Job description

Responsibilities:
  • Ensure departmental or functional training plans in place and appropriate
  • Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget
  • Generate, validate, and/or review SDTM domains and ADaM datasets and associated specifications
  • Generate, validate, and/or review tables, figures and listings to support the statistical analysis of clinical trials data in support of regulatory submissions and publications
  • Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports)
  • Maintain complete and auditable documentation of all programming activities
  • Manage datasets and output across SAS programs, studies, and indications to ensure consistency
  • Manage and provide statistical programming support to supplemental or exploratory analyses for pharmacovigilance, regulatory agencies, or any other internal and external ad-hoc requests
  • Manage programming, testing, and documenting SAS global utility programs and tools in accordance with standards and validation procedures
  • Develop and/or maintain departmental procedures and standards
  • Review CRFs, edit check specifications, and table, figure, and listing mock-ups
  • Manage, generate, and/or review acrf.pdf, define.xml, define.pdf, and reviewer's guide documents
  • ssist in validation of SAS per 21 CFR Part 11
  • Train and mentor new members and programmers; supervise contract programmers, as needed
Requirements:
  • Bachelor's degree in Statistics, Mathematics, Computer Science or a related field required
  • Minimum of 6 years biotechnology/pharmaceutical/CRO industry experience as a statistical programmer
  • Prior experience overseeing statistical programming contractors required
  • Compound oversight experience highly preferred
  • Extensive knowledge of SAS Macros highly preferred, in addition to knowledge of Base SAS, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS
  • Experience working with other languages or software (R, Python, Spotfire) in validated environments is strongly preferred
  • Demonstrates extensive knowledge with industry standards, such as the ICH guidelines, CDISC standards/implementation guides, 21 CFR Part 11, and FDA guidelines
  • eCTD NDA submission experience is a must.

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