Jobs at Cytel

The role involves providing strategic statistical advice, developing innovative solutions for clients in the biopharmaceutical sector, and leading consulting projects to enhance brand recognition and client relationships.

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 design and delivery of end-to-end BI solutions and market-facing analytics tools. Define strategy and roadmaps, translate business needs into requirements, guide development and testing, oversee deployments, ensure data governance, and liaise with stakeholders to prioritize fixes and maintain documentation and compliance.

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.

The Senior Director, Business Development will drive Cytel’s Pharma client relationships, create strategic sales plans, and oversee client-focused initiatives to expand business growth.

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.

Lead and expand Cytel's large pharma accounts by managing global sales teams, creating and executing strategic account and sales plans, driving RFP/RFI responses and proposals, engaging stakeholders across organizations, and representing Cytel at industry events to win clinical trial and biometrics business.

The Executive Consultant will lead strategic consulting in Quantitative Clinical Pharmacology, mentor teams, and engage with clients for business development and scientific expertise.

The Sales Operations Lead defines and executes sales strategies, optimizes operations, partners with executives, and leads high-performing teams to drive revenue growth.

The Head of Quality Assurance will lead Cytel's global QA strategy, enhance the Quality Management System, and drive modernization through digital tools and automation. Responsibilities include managing audits, compliance, and mentoring a high-performing QA team.

The Senior Director, Portfolio Leadership is responsible for revenue growth, solution architecture, and client engagement, ensuring high-value offerings are aligned with client needs and market trends.

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 territory revenue growth by managing full sales cycle, building long-term client relationships, evangelizing Cytel solutions, organizing events, and exceeding quarterly targets through strategic, consultative selling and pipeline management.

The role involves developing and closing software business in clinical research organizations, executing sales strategies, and maintaining client relationships in the biopharmaceutical space.

The Senior Director is responsible for strategic leadership in clinical endpoint adjudication services, ensuring quality delivery, compliance, and operational oversight across global clinical trials.