The Principal Statistician, Biostatistics supports clinical trial design, analysis, and reporting from Phase I to IV, under supervision.
They collaborate with cross-functional teams to optimize study protocols, develop statistical analysis plans, and validate data systems.
Responsibilities include programming, interpreting analyses, preparing regulatory documents, and ensuring quality deliverables from external vendors.
Candidates should have expertise in clinical trial design, statistical methods, and regulatory guidelines, with proficiency in SAS and R.
Qualifications include a master's or Ph.D. in a related field, relevant industry experience, and knowledge of drug development regulations.
Remote work is supported, with competitive compensation, benefits, and opportunities for professional development.