Jobs at ORIC Pharmaceuticals, Inc.

Lead analytical development and product characterization for pharmaceutical molecules in CMC development. Develop and optimize analytical methods, design experiments, operate laboratory instruments, analyze samples, process data, and prepare technical reports and regulatory filing sections. Maintain compliant laboratory records, communicate results, and support multidisciplinary projects. The role requires extensive pharmaceutical or biotechnology research experience, analytical laboratory expertise, and experience in GLP and cGMP environments.

Leads analytical sciences activities across outsourced and in-house pharmaceutical development, including method development, validation, characterization, release and stability testing, investigations, specifications, and regulatory filing support. Manages CDMO and CRO relationships, technical transfers, GMP manufacturing oversight, data review, documentation, budgets, and cross-functional collaboration with Quality, Regulatory, Clinical Supply, and Process Chemistry teams.

Leads biostatistics strategy across clinical development programs, including Phase 3 trial design, statistical analysis plans, data interpretation, regulatory submissions, and health authority interactions. Oversees CROs, vendors, statistical infrastructure, and compliance while mentoring internal and external teams. Partners cross-functionally to support oncology programs, pivotal trials, inspection readiness, and data-driven decision-making.