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 ...
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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 Aug 5, 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.
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?
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.
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.
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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:
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Medical, Retirement, PTO
Re-posted 24 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 73 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
Qualifications
TRAVEL: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Collaborative Culture
Continuous Growth & Development
Other Employee Benefits
Cincinnati Headquarters Experience
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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;
Qualifications
- Bachelor's Degree in Math, Statistics, Life Sciences, or equivalent
- SAS programming knowledge preferred
TRAVEL: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
-
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
-
- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
-
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
-
- A modern corporate campus designed to support collaboration and productivity
- Multiple on-site dining options in the heart of Madison Square
- Free on-site parking
- Convenient access to on-site 24-7 fitness and wellness facilities
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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