Teams at Cytel

Lead statistical strategy and delivery for Phase I-IV clinical trials embedded with a pharmaceutical sponsor. Design analyses, support protocol and reporting activities, oversee programming/CRO work, apply SAS/R (R Shiny)/Python and ML/DL methods for analyses and automation, and mentor junior statisticians.

Perform advanced SAS programming to create and validate safety and efficacy SDTMs and pooled ADaM datasets for ISS and submission packages (define.xml, reviewer's guide). Produce TLFs and ad-hoc reports, apply CDISC standards, support oncology-focused studies, and prepare submission-ready deliverables using Pinnacle 21 and related tools.

Lead design and implementation of SDTM/ADaM specifications, datasets, and Define.xml; develop and validate SAS/R programs for tables, listings, figures and analyses; oversee CRO programming deliverables; support regulatory submissions, study reports, and standards development; collaborate across functions and author SOPs related to statistical programming.