Senior/Principal Statistician Consultant --TA - Oncology (Remote)

Role overview Provide statistical expertise and operational support for oncology clinical trials, helping study teams produce accurate, interpretable, and reproducible analyses. The work spans trial endpoints, data review, statistical deliverables, and coordination with programming and other study partners.

Responsibilities - Support analyses of oncology outcomes, including time-to-event and response-based endpoints, and project event timing for planned analyses. - Review study specifications and deliverables, including SDTM and ADaM plans, tables, listings, figures, analysis plans, protocol updates, and related documentation. - Examine trial data for inconsistencies, missing values, unexpected patterns, and other issues that could affect analysis or interpretation. - Validate statistical outputs and document review steps to support quality control and reproducibility. - Record findings, assumptions, questions, and follow-up actions, and work with study and programming teams to resolve issues.

Requirements - Experience supporting Phase 2 and Phase 3 oncology trials, including event-driven analyses and response-based endpoints. - Working knowledge of CDISC standards, particularly SDTM and ADaM. - Proficiency with statistical programming and data processing tools such as SAS and/or R. - Sound knowledge of statistical methods and experimental design, with a careful approach to data and output review. - Clear written communication for summarizing findings and recommendations; ability to collaborate across study functions. - PhD or equivalent in statistics, biostatistics, or a related field with at least 3 years of relevant experience, or a master’s degree with at least 6 years.

Benefits and work setup - Remote contract engagement supporting clinical study teams. - Availability during core U.S. business hours is expected, generally 9 a.m.–3 p.m. Eastern Time.