Principal Statistical Programmer
- Location
- Uxbridge, England, United Kingdom
behind every successful clinical trial, every regulatory submission, every approved therapy? There's a team of brilliant statistical programmers making sure the data tells the right story, accurately, compliantly, and on time. That's where you come in. So, what will you actually be doing … major regulatory submissions Are deeply fluent in SAS, CDISC/SDTM/ADaM standards, and the end-to-end clinical data pipeline Understand the full drug development lifecycle, from eDC data collection through to TFLs and e-submission components Can hold your ...