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Posted Mar 19, 2026

Principal Biostatistician FSP - Clinical Development

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Job Description As Principal Biostatistician, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-III clinical studies, with a focus on Neurology therapeutic area. This position reports to the Director of Biostatistics in FSP Services business unit in Cytel. Responsibilities You will contribute by: • providing statistical support to clinical studies, with a focus on Neurology; • participating in the development of study protocols, including participation in study design discussions and sample size calculations; • reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications; • performing statistical analyses; • interpreting statistical results; • preparing clinical study reports, including integrated summaries for submissions; • leading study activities when called upon; • utilizing your strong communication skills to present and explain methodology and consequences of decisions in lay terms; • serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.; • being adaptable and flexible when priorities change Qualifications What we're looking for: • Master's degree in statistics or a related discipline. PhD strongly desired. • 5+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. Experience working for a CRO strongly desired. • Experience in sample size calculation, protocol concept development, protocol development, SAP and preparing clinical study reports including integrated summaries for submissions. • Knowledge and implementation of advanced statistical methods. • Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables and working closely with Programmers. Knowledge of R programming a plus. • Strong knowledge of ICH guidelines. • Solid understanding & implementation of CDISC requirement for regulatory submissions. • Adept in ADaM specifications generation and QC of datasets. • Submissions experience • Experience working with cross-functional teams, a Study Management Team (SMT) or similar teams for different clients. • Effective communicator: able to explain methodology and consequences of decisions in lay terms. • Team player; willingness to go the extra distance to get results, meet deadlines, etc. • Ability to be flexible when priorities change and deal with ambiguity