Jobs at Cytel

Lead and manage a team within the Cytel Global Market Access unit, ensuring client satisfaction, project leadership, business development, and operational efficiency. Act as a thought leader in market access and supervise staff while fostering teamwork and continuous improvement.

Lead statistical activities for clinical trials from protocol design through reporting. Provide statistical oversight, collaborate with cross-functional teams and CROs, apply SAS/R (and ML) for analyses, automate processes, and mentor junior statisticians.

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.

Lead EDC database design and builds in Medidata Rave, translating protocol requirements into CRFs, edit checks, derivations, code lists, integrations, and governance. Serve as Medidata SME, maintain core configuration standards, liaise with data management and statistical teams, and provide guidance on platform updates and integrated workflows to support compliant clinical trials.

Design, develop, and maintain clinical EDC databases in Medidata Rave. Translate protocol requirements into CRFs, edit checks, derivations, code lists, user roles, and integrations. Govern core EDC configuration and Cloud Admin roles, review Medidata updates, mentor teams, liaise across data management, biostatistics, and clinical operations, and support integrated clinical data workflows for compliant trial execution.

Lead statistical programming for real-world evidence and epidemiology studies: prepare and link RWD (claims/EHR), implement analytic plans, conduct regression and survival analyses, produce tables/figures, liaise with vendors and stakeholders, and support study reports and presentations.