Cytel Benefits Overview

Lead biostatistical support for Phase I–IV clinical trials, including study design, sample size calculations, exploratory and efficacy analyses, simulation studies, statistical analysis plans, regulatory submissions, and interpretation of results. Provide strategic guidance to cross-functional teams, oversee vendor-supported work, apply advanced statistical methods, and communicate technical findings clearly to technical and non-technical stakeholders.

Leads the organization’s AI program portfolio, overseeing strategic initiative planning, delivery, governance, prioritization, budgets, risks, and performance. Manages AI competitive intelligence activities, vendors, consultants, and strategic partners. Coordinates cross-functional teams and executive stakeholders, facilitates governance meetings, prepares reports and business cases, and ensures AI programs align with corporate objectives and deliver measurable value.

Leads statistical programming for pharmaceutical clinical development studies, generating SDTM and ADaM datasets, specifications, tables, listings, graphs, and regulatory documentation. Develops, validates, and maintains SAS and R programs; supports FDA submissions, clinical study reports, DSURs, publications, and data transfers. Oversees programming deliverables, maintains standards and macros, collaborates with CROs and vendors, and provides technical leadership and mentorship.