Teams at Cytel

Lead sponsor-dedicated statistical programming for clinical trials: create SDTM/ADaM specifications and datasets, develop and validate SAS programs, oversee CRO deliverables, support regulatory submissions and study reports, maintain programming standards, and collaborate across clinical and vendor teams.

Lead or support Phase I-IV clinical trial programming using SAS and CDISC standards to generate and validate SDTM/ADaM datasets, produce TLFs, perform QC/validation, create submission documents (define.xml), and communicate with cross-functional teams. Provide ad-hoc reports, efficacy analyses, and occasional study lead duties while working collaboratively in a global, remote environment.

Lead or support Phase I-IV clinical trial programming using advanced SAS and CDISC (SDTM/ADaM). Produce and validate SDTM/ADaM datasets, TLFs, define.xml and submission documents, perform QC/validation, ad-hoc reporting, efficacy analyses, and collaborate with cross-functional teams. Serve as study lead when required and deliver high-quality outputs on tight timelines.