Jobs at Cytel

Lead and deliver statistical programming for sponsor clinical trials: generate SDTM/ADaM specs and datasets, implement and validate SAS programs, produce tables/listings/figures, oversee CRO programming deliverables, support regulatory submissions and clinical study reports, and develop programming standards, SOPs, and documentation.

Set up and adjust projects and contracts in the accounting system, manage resource assignments and timesheets, maintain contract/milestone/invoicing trackers, monitor and assign ticketing items, compile time reports, and prepare invoicing packages with backup for review.

Design, develop, and maintain BI Publisher, OTBI, and OAC reports and dashboards; modify invoice templates; manage scheduled jobs; build integrations via OIC and APIs; troubleshoot Fusion ERP↔EPM and external vendor integrations; connect OAC to various data sources; manage environment, security, and documentation.

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 statistical programming for sponsor clinical trials: develop SDTM/ADaM specs and datasets, author validated SAS/R programs, oversee CRO deliverables, support regulatory submissions, and maintain programming standards and SOPs.

Lead and perform SAS-based data manipulation, analysis, and reporting for Phase I-IV clinical trials. Develop and validate SDTM and ADaM datasets, produce TLFs, perform QC/validation, generate ad-hoc reports, prepare submission documents (define.xml), support efficacy analyses, communicate with cross-functional teams, and perform study lead duties as needed.

Lead and implement statistical programming for clinical trials: generate SDTM/ADaM/Define.xml, develop and validate SAS/R programs, produce tables/listings/figures, oversee CRO deliverables, support regulatory submissions and clinical study reporting, and maintain programming standards and SOPs.

Lead or support Phase I-IV clinical trial programming: create and validate SDTM/ADaM datasets, produce TLFs and ad‑hoc reports, perform QC/validation, prepare submission documents, liaise with cross‑functional teams, and provide study lead duties as needed.

The Principal Biostatistician leads clinical studies, provides statistical expertise for trial processes, and collaborates with sponsor teams on HTA submissions.

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.