Teams at Cytel

Provides clinical data management support for assigned studies, including ongoing data review, discrepancy resolution, query management, database lock preparation, regulatory documentation, and user access administration in Medidata Rave. Collaborates with clinical operations, biostatistics, programming, and medical monitoring teams to ensure accurate, complete, compliant, and analysis-ready clinical trial data.

Lead real-world evidence biostatistical analyses using large-scale healthcare data to support clinical development, regulatory strategy, HEOR, and payer decisions. Design observational studies and target trial emulations, apply causal inference, statistical learning, machine learning, and NLP, and build reproducible Python/R workflows. Collaborate with clinical, epidemiology, data engineering, and HEOR teams while translating findings for technical and non-technical stakeholders. Support regulatory submissions, governance, audits, and scientific dissemination.

Develop automation and AI solutions supporting pharmaceutical clinical trials. Interpret requirements, identify workflow improvements, build proof-of-concept tools using R, Shiny, and LLM-supported coding, and mature successful prototypes into validated, documented, reusable solutions. Collaborate with statisticians, programmers, data scientists, and AI leads while ensuring testing, traceability, audit trails, version control, and compliance with regulated clinical development expectations.