Statistical Programmer III (R and SAS)

We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in oncology.

The successful candidate will be detail-oriented and motivated to deliver high-quality outputs, with a collaborative and customer-focused mindset. You will work closely with programmers, biostatisticians, and cross-functional teams to support effective data preparation, analysis, and reporting for clinical trials.

This is remote UK and you will need the right to work.

Key Responsibilities:

Data preparation: Program safety and efficacy SDTM and ADaM datasets in compliance with CDISC standards, including RECIST SDTM domains where applicable. Support data mapping, integration, and documentation activities to ensure datasets are analysis-ready.

Anomaly detection: Identify data discrepancies and anomalies within clinical trial datasets through structured review and QC activities. In...