2 of 2 CDISC Jobs in the UK excluding London

/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you • Global exposure • Variety of therapeutic areas • Collaborative and supportive team environment • Access to cutting-edge and More ❯

clinical trial results into value dossier and regulatory submission packages Lead development of statistical programs using SAS for regulatory and non-regulatory submissions (pre-defined and post-hoc) Implement CDISC standards as required for project deliverables Conduct QC programming for descriptive and complex studies in RWD Contribute to writing study reports and use of visualization tools for reporting and data More ❯