Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Create SDTM data via SAS programming by implementing data standards for collected study level source data; * Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
Strong programming and logic skills (working knowledge of SAS) * Ability to apply drug development ... Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from ...
Quick apply
Strong programming and logic skills (working knowledge of SAS) * Ability to apply drug development ... Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from ...
Sdtm Programmer information
See Ohio salary details
$11.43 - $16.33
4% of jobs
$16.33 - $21.23
9% of jobs
$24.76 is the 25th percentile. Wages below this are outliers.
$21.23 - $26.14
17% of jobs
$26.14 - $31.04
13% of jobs
The median wage is $33.90 / hr.
$31.04 - $35.94
13% of jobs
$35.94 - $40.85
10% of jobs
$40.85 - $45.75
9% of jobs
$46.67 is the 75th percentile. Wages above this are outliers.
$45.75 - $50.65
9% of jobs
$50.65 - $55.55
7% of jobs
$55.55 - $60.46
6% of jobs
$60.46 - $65.36
4% of jobs
$11
$37
$65
How much do sdtm programmer jobs pay per hour?
As of Jun 17, 2026, the average hourly pay for sdtm programmer in Ohio is $37.59, according to ZipRecruiter salary data. Most workers in this role earn between $24.47 and $48.89 per hour, depending on experience, location, and employer.
How hard is it to get a job at SAS?
Sdtm Programmers can find opportunities at SAS, especially with strong knowledge of SAS tools, programming skills, and understanding of clinical data standards. Entry-level roles may require relevant certifications or experience, but the hiring process generally depends on the candidate's technical expertise and industry experience. Competition can vary based on location and demand for specialized skills in clinical data management.
What are the key skills and qualifications needed to thrive in the Sdtm Programmer position, and why are they important?
To thrive as an SDTM Programmer, you need a strong background in clinical data management, data standards (especially CDISC SDTM), and programming skills—typically in SAS. Familiarity with SDTM mapping, data validation tools, and relevant regulatory submission platforms or certifications (e.g., SAS Certified Clinical Trials Programmer) is highly valuable. Strong attention to detail, analytical thinking, and effective communication enable collaboration with clinical teams and accurate data interpretation. These skills ensure clinical trial data is accurately standardized, regulatory-compliant, and ready for analysis, which is critical to successful drug development processes.
What is an SDTM Programmer job?
An SDTM Programmer is responsible for converting clinical trial data into standardized Study Data Tabulation Model (SDTM) datasets as per CDISC (Clinical Data Interchange Standards Consortium) guidelines. They ensure that data is structured and formatted correctly for regulatory submissions to agencies like the FDA or EMA. Their work involves writing SAS programs, validating datasets, and collaborating with clinical teams to ensure compliance and accuracy. Strong knowledge of SDTM standards, SAS programming, and clinical trial processes is essential for this role.
Is SAS programming in demand?
SAS programming remains in demand, especially in industries like pharmaceuticals, healthcare, and finance that rely on clinical trial data analysis and regulatory reporting. Skilled SAS programmers with knowledge of data management, statistical analysis, and validation tools are sought after, and proficiency in SAS can lead to stable employment opportunities.
What is the role of SDTM programmer?
An SDTM programmer is responsible for developing and validating data tabulation models (SDTM) for clinical trial data submissions, ensuring compliance with regulatory standards such as CDISC. They use programming languages like SAS or R to transform raw data into standardized formats, supporting accurate data analysis and reporting.
How much do SAS programmers make?
SAS programmers, including SDTM programmers who specialize in clinical data management, typically earn between $70,000 and $120,000 annually, depending on experience, location, and certifications. Entry-level positions may start around $60,000, while senior roles with advanced skills and certifications can exceed $130,000. Salary also varies based on the complexity of projects and the industry sector.
What are the typical daily responsibilities of an SDTM Programmer?
SDTM Programmers are primarily responsible for transforming raw clinical trial data into standardized SDTM domains using programming languages like SAS. On a daily basis, you may be involved in mapping study data to SDTM specifications, validating the datasets, resolving discrepancies with data management teams, and documenting your processes for regulatory review. Collaboration with biostatisticians, clinical data managers, and quality assurance teams is also a significant part of the role. These responsibilities ensure that clinical data is accurate, compliant with industry standards, and prepared for analysis and submission to regulatory agencies.
What are popular job titles related to Sdtm Programmer jobs in Ohio? For Sdtm Programmer jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Sdtm Programmer jobs in Ohio look for? The top searched job categories for Sdtm Programmer jobs in Ohio are:
Other
Medical, PTO
Posted 15 days ago
Medpace rating
8.4
Based on 8 frontline employees who took The Breakroom Quiz
15th of 57 rated research
Job description
Job Summary
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Standard Analyst to join our Biostatistics team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities- Implement edit check specifications via SAS programming to assist with reconciliation of data discrepancies;
- Create annotated CRFs and mapping specifications per CDISC SDTM standards;
- Create SDTM data via SAS programming by implementing data standards for collected study level source data;
- Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
- Ensure SDTM data conforms to the data standards expected by regulatory agencies;
- Assist with creation of the define package for submission to regulatory agencies;
- Bachelor's Degree in Math, Statistics, Life Sciences, or equivalent
- SAS programming knowledge preferred
TRAVEL: None
Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Employment Type: OTHER
About Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992