Senior Principal Statistician, Biostatistics
Seeking an experienced statistician to lead statistical aspects of clinical trials from Phase I to IV, including study design, analysis, validation, and regulatory documentation.
Responsibilities include developing analysis strategies, collaborating across departments, reviewing protocols, creating statistical programs, and supporting regulatory interactions.
Required skills involve expertise in clinical trial design, advanced statistical methods, proficiency in SAS and R, knowledge of regulatory guidelines, and strong communication abilities.
Preferred qualifications include a PhD or MS in related fields, experience with oncology or hematology, Bayesian/adaptive designs, and familiarity with CDISC standards.
This role offers a remote work option with a competitive salary range, benefits, and potential bonuses.