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Clinical sas programmer (sas/r)

Newcastle Upon Tyne (Tyne and Wear)
princeps technologies
Sas programmer
Posted: 30 March
Offer description

Job Title: Clinical SAS Programmer (SAS/R)

Experience: 8+ Years (SAS) | 3+ Years (R)

Location: UK/USA


Job Overview

We are seeking an experienced Clinical SAS Programmer with strong R expertise to join our growing Early Phase SAS Programming team. In this role, you will be responsible for developing, validating, and maintaining SAS and R programs to support clinical trial reporting, data analysis, and visualization.

You will work closely with biostatisticians and cross-functional teams to deliver high-quality outputs that enhance the efficiency, quality, and success of early-phase clinical trials. This role reports to the Early Phase Programming Lead and requires the ability to work independently with minimal supervision.


Key Responsibilities

* Develop, validate, and maintain SAS and R programs for clinical trial data analysis
* Design and build interactive applications using R Shiny
* Convert and optimize programs between SAS and R environments
* Generate Tables, Listings, and Figures (TFLs) for early-phase clinical studies
* Perform oversight and quality control (QC) of vendor deliverables and datasets
* Apply CDISC standards (SDTM, ADaM) in programming and data handling
* Generate and review Pinnacle 21 validation reports and data packages
* Utilize data visualization techniques (R Shiny) to support data-driven decision-making
* Ensure reproducibility by organizing code, data, and outputs into structured repositories
* Prepare and maintain technical and process documentation


Required Qualifications

* 8+ years of experience in Clinical SAS Programming
* 3+ years of hands-on experience in R programming
* Strong experience in R Shiny application development
* In-depth knowledge of CDISC standards (SDTM, ADaM)
* Experience with Pinnacle 21 validation processes
* Proven experience in generating TFLs for clinical trials
* Strong understanding of clinical trial data and regulatory requirements
* Excellent written and verbal communication skills


Preferred Skills

* Experience in early-phase (Phase I/II) clinical studies
* Exposure to data visualization and reporting automation
* Ability to work in a collaborative, fast-paced environment with minimal supervision

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