Overview In this role you will support pharmacometrics by creating and QC’ing NONMEM PK/PD datasets, enabling robust modelling across a global clinical portfolio. You will work with Data Management, Statistical Programming, and Bioanalytical teams to ensure
Overview In this role you will drive CDISC-based data standards within a global clinical operations context. You will support operational staff on ADaM and define.xml capture, build tools to improve data delivery quality, and contribute to
Overview As a Senior Statistical Programmer at ICON, you will develop and validate R programs for statistical analysis of clinical trial data, and lead programming teams to produce CDISC-compliant outputs. You will collaborate with biostatisticians to