Translate advanced analytical plans into robust, efficient, and well-documented code. Support rapid-turnaround analyses, TLF development, and audit-ready outputs while helping build the technical infrastructure behind BSC’s submission-grade delivery.

Lead complex regulatory submissions that set new standards for excellence. Work directly with senior leadership on high-impact programs across medical devices and pharmaceuticals. Contribute to methodological innovation while ensuring FDA-compliant, submission-grade outputs. Ideal candidates hold a Master’s or PhD and bring 5+ years of industry experience with advanced statistical methods.

Support trial design, statistical analysis, and interpretation across a range of clinical programs. Work closely with senior statisticians on SAPs, analyses, and regulatory deliverables while developing deep expertise in FDA-focused biostatistics.