Hiring: Associate Director, CMC Project Management Company: ORIC Pharmaceuticals Inc. Location: South San Francisco, CA Job Posted Time: 2026-09-10 10:59:24 Employment Type: On-site Target Skills & Keywords : Financial Planning, Program Management, Project Management, Regulatory Compliance About the job Experience: •9+ years of experience in biopharma CMC development, with increasing leadership responsibility. •Demonstrated success leading programs through commercialization including NDA filing and launch. •Deep expertise in CMC development, manufacturing, and regulatory requirements. •Proven ability to lead highly cross-functional, matrixed teams. •Strong track record of budget ownership and financial decision-making. Required Skills: •End-to-End CMC Leadership & Cross-Functional Integration •Create and execute against integrated cross-functional project plans, leading the integrated CMC strategy. •Translate program strategy into cohesive development, manufacturing, and supply plans with clear milestones and deliverables. •Drive cross-functional alignment in close partnership with Clinical Development, Regulatory Affairs, Quality, Supply Chain, Commercial, and Finance teams. •Guide and lead project performance, risk and financial management, and issues resolution for functional groups. •Provide direction on requirements to meet internal and external stakeholders’ expectations. •Ensure CMC activities are executed in lockstep with clinical timelines, regulatory milestones, and commercial launch plans. •Serve as the CMC representative on program governance teams, influencing key decisions and trade-offs across functions. Qualifications: •Advanced degree (PhD, MS, or equivalent) in Chemical Engineering, Pharmaceutical Sciences, Chemistry, or related field preferred. Compensation: •$210,000 - $240,000 / year Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!