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# Sr Statistical Programmer

- **Company:** The Clinical
- **Location:** United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clean Code Principles, R (Programming Language), Metadata, SAP (Applications), SAS (Software)
- **Published:** June 24, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=3e54ebb5a8feb531

## About the Role

Do you have experience in Statistics?, Do you have a Master's degree?, * Master's degree or equivalent, along with relevant formal academic/vocational qualifications and a minimum of 5 years of SAS programming experience. Alternatively, a Bachelor's degree with 7+ years of SAS programming experience.

 * A minimum of 3 years of hands-on CDISC implementation experience. Any experience with R programming will be considered a significant plus.
 * Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.
 * Previous involvement as a production or QC programmer at both product and study levels.
 * Strong organizational, interpersonal, leadership, and communication skills.
 * Ability to autonomously manage multiple tasks and projects.
 * In-depth understanding of FDA regulatory guidance around Study Data and Submission, including familiarity with the Study Data Technical Conformance Guide, FDA Data Submission Standards Catalog, and associated requirements.
 * A minimum requirement of a strong understanding of CDISC Metadata Submission Guidelines (MSG), Define standards, CDASH, SDTM, ADaM, and controlled terminology standards., Statistical Programming

## Description

* Conduct a comprehensive review of study documents, including Protocol, CRF, and SAP.
 * Create and assess statistical programs in SAS and/or R to produce CDISC-compliant SDTM and ADaM datasets.
 * Execution of validation and quality control procedures for programs, datasets, and statistical reports, ensuring alignment with study requirements.
 * Development and review CDISC SDTM and ADaM mapping specifications.
 * Produce and review Tables, Figures, and Listings (TFLs) in accordance with the SAP.
 * Review datasets for any pending compliance issues and meticulously document identified issues.
 * Generation and review of submission documents like define.xml, SDTM annotated CRF, and reviewers guide.
 * Generation of utility macros and efficient code writing to streamline programming processes.
 * Communicate effectively within project teams to ensure the timely and budget-compliant completion of assigned tasks.
 * Adherence to Clymb and/or client's Policies and Procedures.


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