Associate Principal Statistical Analyst

Role: Senior Statistical Programmer supporting exploratory-stage oncology clinical trials, with responsibilities including technical oversight of programming resources, ensuring quality and timely analysis deliverables, and supporting regulatory submissions. The position may lead specific phases or programs within early or late-phase oncology studies. Responsibilities encompass managing CROs, mentoring team members, ensuring compliance with CDISC standards, and maintaining regulatory standards such as GxP and 21 CFR Part 11. Requirements include 10-14 years of statistical programming experience in biotech/pharma, a relevant BS/BA degree, and proven expertise in supporting clinical trial analysis datasets, tables, listings, and figures. Preferred qualifications involve experience in oncology trials and demonstrated leadership skills. High-value specifics involve supporting late-stage oncology programs targeting RAS mutations with biologics or small molecules, from early to late phases, with regulatory, GxP, and CDISC compliance. The role reports to senior management, with a focus on collaboration across clinical and regulatory functions. Work setup is onsite at Redwood City, CA, with salary range $164,000-$205,000 USD, and may require multi-tasking and strategic problem-solving in a high-energy environment.