Senior Director, Patient Reported Outcomes

Role: Senior Director, Patient-Reported Outcomes (PRO) leads the scientific strategy for integrating patient-centered outcomes into clinical development, supporting regulatory and market access goals. Responsibilities: develop and execute PRO strategies, select and validate PRO measures, collaborate with cross-functional teams to embed PRO endpoints into study designs, and generate PRO evidence for regulatory submissions and scientific communications. Provides methodological guidance on PRO data analysis and interpretation, and engages with regulatory authorities and external stakeholders. Qualifications: Ph.D., M.D., or equivalent in health outcomes, psychology, or related field; minimum 13 years' experience in PRO, health outcomes research, or patient-focused drug development within pharma, biotech, CRO, or academia. Skilled in qualitative and quantitative PRO methodologies, regulatory expectations, and cross-functional collaboration. Preferred: oncology PRO experience, especially in RAS-driven cancers, late-stage development support, and experience with external research partners. High-Value: Oncology focus, clinical development stages (late Phase 2/3), regulatory engagement, global health authority expectations, and expertise in patient-centered outcome assessments. Work Setup: Full-time, based in Redwood City, CA, with salary range $232,000–$290,000, including comprehensive benefits and equity; specific location-based details provided.