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Navitas Life Sciences

Senior Statistical Programmer

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer ... Critical client project activities are reporting database development (SDTM and ADaM), statistical ...

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer ...

Systimmune

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

The Statistical Programmer will support statistical programming activities for clinical trials ... Generate and/or validate SDTM and ADaM datasets, including associated Define.xml and reviewer ...

ImmunityBio, Inc.

Principal Statistical Programmer

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 ...

IQVIA

Principal Statistical Programmer

Durham, NC · On-site

$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 ...

VENESCO, LLC

SAS Programmer

Falls Church, VA · On-site +1

Develop SAS programs for tables, listings, and figures (TLFs) Create CDISC-compliant datasets (SDTM and ADaM) Validate and document programming outputs Collaborate with statisticians and data ...

VENESCO LLC

SAS Programmer

Falls Church, VA · On-site

Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs • ...

Venesco LLC

SAS Programmer

Falls Church, VA · On-site

Requirements Key Responsibilities: • Develop SAS programs for tables, listings, and figures (TLFs) • Create CDISC-compliant datasets (SDTM and ADaM) • Validate and document programming outputs ...

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How much do sdtm programmer jobs pay per hour?

As of Jul 21, 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.

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.

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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Sdtm Programmer jobs near you
Infographic showing various Sdtm Programmer job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 7% Part Time, 1% Temporary, 6% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.
Senior Statistical Programmer

Senior Statistical Programmer

Navitas Life Sciences

Remote

Full-time

Posted 15 days ago

Job description

Job Description
The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory submissions and publications.
Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support.
About the Role
  • Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures and tables;
  • Independently, develop SAS application code;
  • Independently, perform validation of SAS programs and deliverables;
  • Independently, perform migrations and verifications;
  • Independently, perform SDTM and ADaM mapping;
  • Generate SDTM and ADaM deliverables;
  • Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and ISE;
  • Generate data files and/or output for safety updates, publications and meeting presentations;
  • Interface with a cross-function of client and DataCeutics team members; and
  • Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.

Desirable Skills and Experience
  • Background in statistics and statistical analysis is desirable
  • 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming
  • Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming
  • Working knowledge of CDISC, SDTM and ADaM
  • Expert knowledge of SAS-based statistical programming
  • Proficiency in SAS programming on multiple platforms and operating systems, e.g. Windows, UNIX, etc. is desirable

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