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Clinical Statistical Programmer Jobs in Ohio (NOW HIRING)

Medpace, Inc.

Statistical Analyst I

Cincinnati, OH

SAS and / or statistical programming experience; * Knowledge of databases and data management process; and * Knowledge of statistical methods commonly used in pharmaceutical clinical trials. Travel:

Medpace, Inc.

Statistical Analyst I

Cincinnati, OH · On-site

SAS and / or statistical programming experience; * Knowledge of databases and data management process; and * Knowledge of statistical methods commonly used in pharmaceutical clinical trials. Travel:

Fortrea

Principal Biostatistician - FSP

Toronto, OH · On-site +1

$115K - $130K/yr

... complex clinical trials for renowned, innovative and global top pharmaceutical and biotech ... and review Statistical Analysis Plans for data presentation, analyses, and provide programming ...

Medpace, Inc.

Biostatistician I

Cincinnati, OH

Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies; * Programming of study analysis, review of study results and ...

Medpace, Inc.

Biostatistician I

Cincinnati, OH · On-site

Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies; * Programming of study analysis, review of study results and ...

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

Required : • BS in Statistics, Mathematics, Life Sciences, or related field • SAS Programming experience required • Minimum 3.4 GPA Company : Medpace, Inc., a clinical research organization ...

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Clinical Statistical Programmer information

See Ohio salary details

$15

$51

$85

How much do clinical statistical programmer jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical statistical programmer in Ohio is $51.51, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $77.45 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Statistical Programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a Clinical Statistical Programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a Clinical Statistical Programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What Does a Clinical Statistical Programmer Do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

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Clinical Statistical Programmer jobs near you

Statistical Analyst in Cincinnati, OH (Fulltime only, No C2C)

Northern Base

Cincinnati, OH • On-site

Full-time

Posted 4 days ago

Job description

Senior Statistical Analyst
Cincinnati, OH
Fulltime
 
Required Skillsets:
Proficiency in SAS / R programming languages to Program and validate ADaM, TFL and statistical analyses
Proficiency in using statistical software and programming tools
Understanding of statistical methods, data analysis techniques, and clinical research processes.
Advance knowledge of CDISC standards and therapeutic area (Oncology, Immunology, Neuroscience etc.)
Strong attention to detail and quality Focus
Problem-solving skills (Ability to identify and troubleshoot programming issues) 
Effective communication skills (both written and verbal)
Ability to interact professionally with statisticians, study teams, and external partners
Ability to work collaboratively in a team environment and adapt to changing priorities and deadlines.
 
Key Responsibilities:
1. Collaborate with statisticians to develop, review, and approve Statistical Programming Plans (SPP).  Implement Statistical Analysis Plans (SAP) and SPP to create ADaM data specifications.
2. Program and validate ADaM and statistical analyses using programming languages (e.g., SAS, R), ensuring adherence to established standards and guidelines.
3. Generate tables, listings, and figures (TLFs) for clinical study reports, safety reports, and other deliverables, ensuring accuracy, consistency, and adherence to regulatory requirements.
4. Develop and maintain programming documentation, such as annotated program code, programming specifications, and validation plans.
5. Perform quality control checks on statistical programming deliverables to ensure accuracy, consistency, and adherence to programming standards.
6. Collaborate with cross-functional teams to support ad hoc data analyses, data visualization, and exploratory analyses as needed.
7. Ability to lead the development and implementation of standard programming macros, utilities, and tools to improve efficiency and consistency in programming tasks.
8. Stay updated with industry best practices, regulatory guidelines, and emerging technologies in statistical programming and data analysis.
9. Lead the planning and execution of statistical programming-related audits, inspections, and regulatory submissions, ensuring compliance with relevant regulations and guidelines.
10. Collaborate with statisticians and study teams to provide programming support, address data-related queries, and contribute to study-related publications.
11. Performs assigned task(s) in accordance with customer requirements within agreed timelines and Quality.
12. Escalates unresolved issues appropriately to Team Lead /Project Lead. Tracks and follows up on all issues raised. Provides timely status updates. Proactively highlight risk.
13. Coach/Mentor/Train new team members and line function as per requirement.