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Cdisc Sdtm Jobs (NOW HIRING)

Servier

Sr. Manager, Statistical Programming

Boston, MA · On-site

$151K - $172K/yr

Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM standards * Ensure the datasets (SDTMs and ADaMs) are CDISC compliant * Keep abreast of current and new ...

Fortrea

Clinical data Spec- Coordinator

San Jose, CA · On-site

Familiarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM) * Strong attention to detail and problem-solving skills * Effective communication and collaboration abilities * Ability to ...

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Uphold industry standards including protocol compliance, ICH GCP, FDA regulations, and CDISC standards (SDTM, ADaM). Qualifications: * Bachelor's degree in Biostatistics, Computer Science, Life ...

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How much do cdisc sdtm jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for cdisc sdtm in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Cdisc Sdtm position, and why are they important?

To thrive as a CDISC SDTM specialist, you need a deep understanding of clinical data management, strong knowledge of CDISC standards (particularly SDTM), and experience with statistical programming languages such as SAS. Familiarity with industry tools like Pinnacle 21, Medidata Rave, and relevant CDISC certifications is highly valued. Attention to detail, analytical thinking, and effective communication skills help distinguish top performers in this role. These capabilities are crucial for ensuring the accurate, compliant, and efficient transformation of clinical trial data into standardized formats for regulatory submission.

What is a CDISC SDTM job?

A CDISC SDTM job involves working with clinical trial data to ensure it complies with the Study Data Tabulation Model (SDTM) standard set by the Clinical Data Interchange Standards Consortium (CDISC). Professionals in this role transform raw clinical data into standardized SDTM domains for regulatory submissions to agencies like the FDA. Responsibilities typically include data mapping, programming (using SAS), validation, and documentation. This role is crucial for ensuring data integrity, consistency, and compliance in clinical research.

What does a typical day look like for a CDISC SDTM specialist?

A typical day as a CDISC SDTM specialist involves mapping raw clinical trial data to SDTM standards, collaborating closely with data managers, biostatisticians, and clinical programmers to resolve data issues, and validating data sets for consistency and compliance. You may also participate in meetings to discuss project progress, handle quality control checks using specialized software, and prepare documentation for regulatory submissions. The role often requires balancing independent programming work with teamwork across various functions in a dynamic, deadline-driven environment. This diverse set of tasks provides an engaging workday for those who enjoy both problem-solving and cross-functional collaboration.

More about Cdisc Sdtm jobs
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Cdisc Sdtm jobs near you
Infographic showing various Cdisc Sdtm job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 58% In-person, 4% Hybrid, and 38% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

Clinical SAS Programmer

Interon IT Solutions

Chantilly, VA • Remote

Contractor

Posted 2 days ago

Job description

#W2 Role

Job Title: Clinical SAS Programmer

No of positions- 2

Location- Remote
Experience Required:6+ Years
Education: Bachelor’s degree in Computer Science, Computer Engineering, or related technical field
 

Job Summary

We are seeking a Clinical SAS Programmer with strong experience in SAS programming and CDISC standards within a regulatory environment. The ideal candidate will be responsible for creating and validating SDTM domains and ADaM datasets, developing mapping specifications, and supporting clinical data programming activities with accuracy and compliance.

Key Responsibilities

  • Develop and validate specifications for creating SDTM domains from raw/source clinical data.
  • Create and validate CDISC-compliant SDTM domains and ADaM datasets using SAS.
  • Prepare mapping specifications from CRF and other raw data sources to appropriate SDTM domains.
  • Develop specifications to map SDTM datasets to ADaM datasets.
  • Write clear and detailed programming instructions for complex data derivations.
  • Perform dataset validation and quality checks to ensure regulatory compliance and data integrity.
  • Develop SAS macros and reusable programs to improve efficiency and streamline workflow.
  • Apply advanced SAS programming techniques for custom clinical data programming needs.
  • Work effectively in a dynamic environment and adapt quickly to changing project requirements.

Required Qualifications

  • Bachelor’s degree in Computer Science, Computer Engineering, or a related technical field.
  • 4+  years of experience in clinical SAS programming.
  • Strong hands-on experience using SAS to create CDISC-compliant outputs in a regulated clinical environment.
  • Solid understanding of SDTM, ADaM, and clinical data standards.
  • Experience in writing and validating dataset specifications.
  • Familiarity with P21 software.
  • Excellent written and verbal communication skills.

Preferred Qualifications

  • Experience with R and Python is a strong plus.
  • Ability to work independently and collaboratively within cross-functional teams.
  • Strong attention to detail and problem-solving skills.