Teams at Cytel

Leads statistical programming for pharmaceutical clinical development studies. Develops and validates SAS and R programs, SDTM and ADaM datasets, tables, listings, figures, Define.xml files, and regulatory submission deliverables. Oversees CRO programming work, supports clinical reports and regulatory interactions, maintains programming standards, contributes to CRF and validation planning, and collaborates with clinical, statistical, vendor, and regulatory teams.

Performs SAS programming, data manipulation, analysis, reporting, and QC for Phase I–IV clinical trials. Generates and validates SDTM and ADaM datasets, tables, listings, figures, ad hoc reports, submission documents, and eCRTs. Supports efficacy and safety analyses, communicates with cross-functional teams and clients, contributes to study leadership, and delivers compliant outputs within challenging timelines.

Independently leads statistical programming for pharmaceutical clinical development studies. Develops and validates SAS and R programs, SDTM and ADaM datasets, specifications, tables, listings, graphs, and regulatory submission deliverables. Oversees CRO programming work, supports clinical study reports and FDA submissions, maintains programming standards, contributes to CRFs and validation plans, and collaborates with clinical, regulatory, vendor, and development teams.