Principal Biostatistician

Overview

This role provides comprehensive statistical support across all phases of clinical development. Responsibilities involve writing and reviewing statistical protocol sections and analysis plans, performing statistical analyses, presenting results to sponsors and project teams, and developing SAS programs for tables, listings, figures, and datasets.

Who can apply

Applicants must hold either a Master's degree or equivalent in Statistics, Biostatistics, or a related field along with ten or more years of experience, or a PhD in Statistics, Biostatistics, or a related field with at least seven years of experience. Candidates are required to have experience using SAS and knowledge of industry standards such as FDA guidelines, ICH guidelines, CDISC data structures, and 21 CFR Part 11. Preferred qualifications include experience with rare diseases and oncology, late phase studies or submissions, and client consulting on study designs. Candidates must possess legal authorization to work in the country of employment without employer sponsorship.