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# Senior Statistical Programmer (CDISC SDTM/ADaM)

- **Company:** DBV Technologies
- **Location:** United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Coherent Remote File System (CRFS), SAS (Software)
- **Published:** August 4, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=41319e190e3adc39

## About the Role

* Master's degree (MSc) or PhD in Biostatistics, Statistics, Mathematics, or a related field (e.g., ENSAI or equivalent).
 * Minimum of 6-8 years of experience in statistical programming for clinical trials, with strong expertise in CDISC standards (SDTM/ADaM).
 * Experience with regulatory submissions and CRO management is highly desirable.

Technical Skills

 * Proficiency in SAS (Base SAS, SAS Studio, SAS Viya).
 * Strong expertise in CDISC SDTM and ADaM standards.
 * Good knowledge of TLFs (Tables, Listings, and Figures) and regulatory requirements.
 * Experience using Pinnacle 21.
 * Solid understanding of clinical statistics.
 * Fluent English (written and spoken).

## Description

Provide support for clinical studies through dual expertise in statistical programming compliant with CDISC standards (SDTM/ADaM) and applied biostatistics. The role includes the production, validation, and review of CDISC deliverables, as well as the execution and support of statistical analyses., * Participate in the design of clinical studies in collaboration with biostatisticians.

 * Contribute to the writing and review of Statistical Analysis Plans (SAPs).
 * Program and validate SDTM and ADaM datasets.
 * Produce, validate, and review SDTM/ADaM deliverables (annotated CRFs, specifications, datasets).
 * Ensure regulatory compliance using Pinnacle 21.
 * Participate in and validate regulatory submission deliverables (Define.xml, submission packages).
 * Perform Quality Control (QC) activities.
 * Produce and validate Tables, Listings, and Figures (TLFs).
 * Collaborate closely with clinical and regulatory teams.


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