Jobs at Cytel

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.

Manage sponsor-dedicated clinical development projects for a pharmaceutical client. Coordinate clinical data standards and statistical programming, operational transitions, documentation, inspection readiness, SOP updates, project plans, risks, resources, and stakeholder communications. Facilitate cross-functional collaboration among Data Management, Biostatistics, Statistical Programming, and Clinical Operations teams while supporting process optimization and operational transformation.

The Senior Revenue Accountant owns global revenue recognition and reporting across three business units. Responsibilities include month-end close, percentage-of-completion revenue calculations, contract review, ASC 606 and US GAAP compliance, account reconciliations, controls, audit support, executive reporting, and process improvements. The role collaborates extensively with Finance, Legal, Sales Operations, Commercial Operations, and business development teams.

Supports epidemiology and real-world evidence studies by preparing claims and EHR data, developing analytical databases, programming statistical analyses, creating algorithms, linking datasets, and producing tables, figures, reports, and presentations. Partners with epidemiologists, statisticians, vendors, clients, and internal stakeholders across Medical Affairs, Patient Safety, Risk Management, and Clinical Development. Requires expertise in SQL, SAS or R, RWE data sources, applied statistics, and project management.

Provides technical and functional leadership for epidemiological and real-world evidence statistical programming. Leads hands-on development and validation of SAS and R programs, analysis datasets, tables, figures, and reproducible workflows using healthcare data. Mentors programmers, oversees internal and CRO deliverables, establishes standards and quality processes, supports regulatory and scientific outputs, and collaborates with epidemiologists, statisticians, and data scientists across projects and therapeutic areas.

Supports epidemiology and real-world evidence studies by preparing claims and EHR data, developing analytical databases, conducting statistical analyses, and producing tables, figures, reports, and presentations. The role assists with protocols and analysis plans, coordinates with data vendors and stakeholders, applies regression and survival methods, and supports Medical Affairs, Patient Safety, Risk Management, and Clinical Development initiatives. Strong SQL, SAS, or R expertise and experience with pharma RWE analytics are required.