Teams at Cytel

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.