• Define and drive multi-year product strategy and roadmap across one or more RIR components, ensuring alignment to clinical quality, regulatory requirements, and commercial scale objectives • Influence platform-level technical direction in partnership with engineering leadership • Partner closely with software engineering, bioinformatics, clinical domain experts, quality, regulatory, and other product teams • Translate business, clinical, and operational needs into clear, actionable product requirements • Define and evolve end-to-end user workflows, including UI/UX requirements and supporting backend functionality • Drive cross-team alignment on shared data contracts and workflow standards • Mentor and raise the bar for product management within the RIR organization • Own measurable improvements in clinical workflow efficiency, reliability, and operational scalability • Establish prioritization frameworks that balance regulatory risk, clinical impact, technical scalability, and business outcomes across RIR investments. • Develop and track quantitative metrics related to usability, performance, reliability, and adoption • Lead delivery teams with clear strategic direction, ensuring requirements reflect long-term platform goals, validation readiness, and system interoperability. • Proactively identify systemic risks, architectural constraints, and workflow inefficiencies that may limit scale or regulatory robustness, and lead cross-functional initiatives to resolve them • Partner with Quality and Regulatory leadership to shape validation strategy, risk classification, traceability, and audit readiness for RIR software systems. • Create clear, data-driven written proposals and presentations to support stakeholder alignment and decision-making • Act as a subject matter expert for owned components, supporting design, testing, validation, rollout, and ongoing use