Jobs at Cytel

Design and deliver R-based data and analysis solutions for clinical trials. Develop reusable R packages, visualizations, and tools; gather requirements; support change management, training, and cross-team collaboration within regulated environments.

Lead statistical programming for clinical trials: generate SDTM/ADaM datasets and Define.xml, develop/validate SAS (and R) programs, oversee CRO deliverables, support regulatory submissions, and maintain programming standards and SOPs.

The Senior Director of Business Development will drive Cytel's Large Pharma expansion by managing client relationships, executing sales strategies, and leading proposal development.

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

Lead strategic statistical consulting engagements, design innovative statistical and clinical development solutions, build client relationships, grow business, mentor consulting teams, represent Cytel externally, and travel regularly to engage senior stakeholders.

The Principal Statistical Programmer will generate specifications and datasets, develop and validate SAS/R programs, oversee CRO deliverables, and ensure compliance with regulations for clinical studies.

Transform operational data into actionable insights by building semantic models, reporting solutions and metrics (Power BI/Fabric, DAX, M, SQL). Ensure data quality, governance, access controls, troubleshooting, documentation, and stakeholder collaboration to enable self-service analytics.

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.

Lead or support Phase I-IV clinical trial programming using SAS and CDISC standards to generate and validate SDTM/ADaM datasets, TLFs, and submission documents. Perform production and QC/validation programming, complex ad-hoc reports, and efficacy analyses while coordinating with cross-functional teams and serving as study lead when required.