Bridge Bio Inc. is seeking a Director of Statistical Programming to lead programming activities for multiple clinical studies and regulatory submissions, performing hands‑on work while guiding CRO deliverables and cross‑functional collaboration. The role requires 10+ years in statistical programming (MS), deep CDISC FDA knowledge, and experience in NDA/BLA submissions. You will establish SAS environments, advance automation with AI tools, and drive standards across the organization.

Also on the board Same function, level within a rung

Level

Manager

Location

Millbrae, CA

Occupation

Biostatisticians

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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