Teams at Cytel

Manage the global end-to-end pass-through accounting process across entities and geographies. Responsibilities include transaction accounting, revenue recognition support, month-end close, journal entries, reconciliations, variance analysis, financial reporting, audit support, internal controls, process documentation, and ERP transformation initiatives. The role partners with Finance, Tax, Treasury, Procurement, Operations, Shared Services, and external stakeholders while ensuring compliance with US GAAP, IFRS, and company policies.

Lead or support Phase I-IV clinical trial statistical programming using SAS, including clinical data manipulation, efficacy and safety analysis, SDTM and ADaM dataset development, TLF generation, QC, validation, ad-hoc reporting, and regulatory submission documentation. The role requires collaboration with cross-functional pharmaceutical teams, potential study leadership, troubleshooting, and delivery of high-quality outputs under challenging timelines.

The Principal Statistical Programmer develops and validates SAS and R programs, SDTM and ADaM datasets, specifications, tables, listings, graphs, Define.xml files, and reviewer’s guides for clinical trials. The role supports regulatory submissions, clinical study reports, data validation, CRF and edit-check development, vendor data transfers, and CRO oversight. It requires extensive oncology expertise, independent ownership of multiple studies, compliance with FDA and CDISC standards, and collaboration across global clinical development teams.