Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Minimum of 10+ years of statistical programming experience in the life science industry and ...
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Minimum of 10+ years of statistical programming experience in the life science industry and ...
Knowledge of SDTM, ADaM, FDA and ICH guidance * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Sr SAS Programmer Analyst - SDTM * Responsible for SDTM data creation and delivery for oncology studies. * Prepare ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Sr SAS Programmer Analyst - SDTM * Responsible for SDTM data creation and delivery for oncology studies. * Prepare ...
Contribute to the creation and review of programming specifications for SDTM and ADaM like datasets based on CDISC standards and internal guidelines. Assist in programming support for data cleaning ...
Contribute to the creation and review of programming specifications for SDTM and ADaM like datasets based on CDISC standards and internal guidelines. Assist in programming support for data cleaning ...
Sr. Statistical Programmer
Omaha, NE · On-site
Ensures that statistical deliverables (tables, figures, listings) and study datasets (SDTM, ADaM ... Develops programming efficiencies (eg, local macros) to ensure efficient programming work
Sr. Statistical Programmer
Omaha, NE · On-site
Ensures that statistical deliverables (tables, figures, listings) and study datasets (SDTM, ADaM ... Develops programming efficiencies (eg, local macros) to ensure efficient programming work
Knowledge of SDTM, ADaM, FDA and ICH guidance * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Knowledge of SDTM, ADaM, FDA and ICH guidance. Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
As a Senior Statistical Programmer, you'll have the opportunity to design and write program ... Extensive experience and understanding in SDTM model including transforming raw data files while ...
As a Senior Statistical Programmer, you'll have the opportunity to design and write program ... Extensive experience and understanding in SDTM model including transforming raw data files while ...
A CDISC SDTM specialist is a key team member on CDISC submission topics; provide industry leading CDISC expertise and programming leadership. They contribute to process improvements and initiatives ...
A CDISC SDTM specialist is a key team member on CDISC submission topics; provide industry leading CDISC expertise and programming leadership. They contribute to process improvements and initiatives ...
Lead Statistical Programmer
Tarrytown, NY · On-site
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Lead Statistical Programmer
Tarrytown, NY · On-site
Knowledge of SDTM, ADaM, FDA and ICH guidance. * Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in ...
Clinical SAS Programmer
Newark, NY · On-site
... Lead programming efforts supporting clinical studies and regulatory deliverables Develop and ... SDTM and ADaM datasets in alignment with CDISC standards Produce high-quality analysis outputs ...
Clinical SAS Programmer
Newark, NY · On-site
... Lead programming efforts supporting clinical studies and regulatory deliverables Develop and ... SDTM and ADaM datasets in alignment with CDISC standards Produce high-quality analysis outputs ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Clinical SAS Programmer
Newark, NY · On-site
Lead programming efforts supporting clinical studies and regulatory deliverables ... Develop and validate SDTM and ADaM datasets in alignment with CDISC standards * Produce high ...
Clinical SAS Programmer
Newark, NY · On-site
Lead programming efforts supporting clinical studies and regulatory deliverables ... Develop and validate SDTM and ADaM datasets in alignment with CDISC standards * Produce high ...
Clinical SAS Programmer
Santa Clara, CA · On-site
This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs * Develop and validate SAS programs ...
Clinical SAS Programmer
Santa Clara, CA · On-site
This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs * Develop and validate SAS programs ...
Summary The Senior Clinical Programmer Contractor will be responsible for support of team data review, data reconciliation and edit checks, and programming submission ready SDTM deliverables. This ...
Summary The Senior Clinical Programmer Contractor will be responsible for support of team data review, data reconciliation and edit checks, and programming submission ready SDTM deliverables. This ...
SeniorEDC Programmer
Bothell, WA · On-site
Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where ... Oversee and/or mentor junior programmers or external vendors. * Contribute to SOP development and ...
SeniorEDC Programmer
Bothell, WA · On-site
Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where ... Oversee and/or mentor junior programmers or external vendors. * Contribute to SOP development and ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Principal Statistical Programmer
$98K - $273K/yr
Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... SDTM datasets * ADaM datasets * Tables, Listings, and Figures (TLFs) * Ensure all deliverables are ...
Principal Statistical Programmer
$98K - $273K/yr
Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... SDTM datasets * ADaM datasets * Tables, Listings, and Figures (TLFs) * Ensure all deliverables are ...
Sdtm Programmer information
See salary details
$12.02 - $17.18
4% of jobs
$17.18 - $22.33
9% of jobs
$26.04 is the 25th percentile. Wages below this are outliers.
$22.33 - $27.49
17% of jobs
$27.49 - $32.65
13% of jobs
The median wage is $35.66 / hr.
$32.65 - $37.81
13% of jobs
$37.81 - $42.96
10% of jobs
$42.96 - $48.12
9% of jobs
$49.09 is the 75th percentile. Wages above this are outliers.
$48.12 - $53.28
9% of jobs
$53.28 - $58.44
7% of jobs
$58.44 - $63.59
6% of jobs
$63.59 - $68.75
4% of jobs
$12
$39
$68
How much do sdtm programmer jobs pay per hour?
As of Jun 28, 2026, the average hourly pay for sdtm programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 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.
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Other
Posted 19 days ago
Job description
Job Title
Responsibilities:
Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets.
Following statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, writes specifications for analysis datasets.
Following specifications, develops algorithms and writes programs to create datasets.
Produces data listings, summary tables and graphs using SAS software.
Independently check data listings, summary tables and graphs.
Imports and exports SAS data.
Assists data management group in performing data edit checks.
Understands and conducts work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and training, and international regulatory requirements.
Plays an active role in taking project solutions and generalizing them for the Biostatistics group.
Interact with the project statistician and guides other programmers participating on a project team.
Experience with Pooled analysis, regulatory agencies requirements and e-submission experience.
Requirements:
Minimum of 10+ years of statistical programming experience in the life science industry and relevant bachelor's degree
Must have recent NDA submissions experience.
ISS/Client safety & efficacy experience is required.
Experience creating define.xml and experience with Pinnacle 21 and specifications.
SAS Certified Base and/or Advance Programmer experience is preferred.
Proven experience in SAS programming including base SAS, SAS/Stat, SAS/Graph, macros, ODS.
Experience with SDTM and ADaM industry data standards.
Good communication skills and attention to detail are crucial.
Proven ability to handle multiple tasks.
Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information.
About Katalyst Healthcares & Life Sciences
Sourced by ZipRecruiter
Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
South Plainfield, NJ, US