> Markdown version of [/jobs/ext/4397589-principal-statistical-programmer](https://www.wearedevelopers.com/jobs/ext/4397589-principal-statistical-programmer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md).

---

# Principal Statistical Programmer

- **Company:** Clinvia LLC
- **Location:** United States (Remote available)
- **Salary:** $127,067.0
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Clinical Data Repository, Computer Programming, Data Validation, SAP (Applications), SAS (Software), SAS/Base, SAS/STAT, SQL Databases, Macros, Data Management
- **Published:** October 15, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=7ce5c8c2f1528c47

## About the Role

* Minimum 12 years Pharmaceutical/Biotech programming experience.
 * NDA submission experience and knowledge required.
 * Strong SAS programming and Statistical background along with experience with SAS Base, SAS/Macros, SAS/Graph and SAS/Stat.
 * Education Requirements (degree, certifications, etc.): Include must have and preferred BS/MS in Statistics, Math or Scientific Discipline.

## Description

* Project lead level activities.
 * Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data.
 * Create CDISC SDTM and ADaM files, SAS export files and Define.xml use for Electronic Submission from the data received in non-standard form from various sources.
 * Performs Data analysis, statistical analysis, generate safety and efficacy tables, listings and graphs using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS.
 * Review Data Management Plan, Data validation plan and edit check specifications
 * Interact with Statisticians and other clinical teams, perform ad hoc analysis and generate outputs according to the requirements.
 * Implements and contributes to statistical analysis plans; provides additional expertise in the analysis of clinical trial as it relates to protocol development, case report form design and data collection.
 * Recognizes inconsistencies and initiates resolution of data problems.
 * Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results.
 * Works on significant and unique issues where analysis of situations or data requires evaluation of intangibles.
 * Acts independently to determine methods and procedures on new assignments.
 * May provide guidance to other lower level personnel.
 * Works closely with Biostatistics to create analysis files specifications following the instructions provided in Statistical Analysis Plan (SAP)
 * Develop SAS coding and table templates for preparing, processing and analyzing clinical data.
 * Create/acquire tools to improve programming efficiency or quality.
 * Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
 * Experience with integrated summaries (ISE/ISS) and Clinical Study Reports.