• Own the end-to-end claims configuration function, including benefits and plan design, pricing logic, accumulator logic, provider data, edits, networks, and adjudication rules • Establish configuration standards, including maintenance of standard codes, naming conventions, and benefit category architecture • Create and maintain a user-friendly configuration documentation library in Gravie’s knowledge management system • Maintain a well-organized configuration task management system • Implement appropriate controls and governance to ensure configuration changes are quality assured • Translate product, regulatory, and contractual requirements into scalable and repeatable configuration solutions • Serve as the subject matter expert on claims configuration capabilities and limitations • Ensure timely and accurate configuration for new products, clients, renewals, and benefit changes • Drive continuous improvement in configuration quality, turnaround time, and defect reduction • Partner with Claims Operations to minimize configuration-driven claim errors • Support root cause analysis of claims issues tied to configuration and implement corrective actions • Collaborate closely with Product, Optimization, Network, Finance, Compliance, Eligibility & Enrollment, and Technology • Create and maintain a balanced scorecard of cost, quality and time metrics with goals • Support product innovation by enabling new benefit designs and network offerings • Partner with Technology on enhancements, automation, testing frameworks, and release management related to systems used for claims processing • Lead, coach, and develop a team of claims configuration professionals • Define roles, workflows, and capacity models to support scale and growth • Support training efforts to ensure configuration knowledge is institutionalized • Ensure configurations comply with regulatory requirements, contractual obligations, and internal policies • Support audits, quality reviews, and regulatory inquiries related to claims configuration • Maintain strong documentation and change management practices to support transparency and traceability

• Drive game related research and development • Develop new tech that enables immersive storytelling in games • Collaborate with technical leadership across multiple games • Build a roadmap of feature exploration • Grow a team of engineers to deliver new technologies

• Manage university partnerships and build strategic relationships • Lead partner strategy and coordinate internal teams • Drive results across enrollment, revenue, and satisfaction • Own full sales and renewal cycle for partnerships • Ensure partner satisfaction and identify risks

• Reporting to the SVP, Drug Safety and Pharmacovigilance, the Senior Director is responsible for supporting the development and implementation of a risk management system for risk detection, risk assessment and risk minimization for investigational and marketed products. • Oversee risk management plan activities including signal tracking maintenance, ad hoc Health Authority requests and the planning and preparation for aggregate safety reports including DSURs, PADERs and PBRERs for Nuvalent’s products. • Close collaboration with DSPV Safety Physicians to analyze potential safety issues, including signal detection, signal evaluation and signal management. • Collaborate proactively with study teams, cross-functional team members, external business partners and vendors to apply knowledge and analytical skills to problems in specific therapeutic areas. • Assist in the evaluation of potential safety issues and quality risk assessment reports. • Coordinate and develop Risk Management Plans for Nuvalent’s products among multiple stakeholders. • Manage and support the authoring for aggregate safety reports (e.g., DSUR, PBRER, PADER) in close collaboration with clinical, medical writing and operational functions.