• Analysing data or insights to determine industry and consumer trends regarding the product and category • Creating and developing a long term plan for the development of the category • Overseeing a team of analysts and other support staff • Becoming a leader in category ranging and promotions across channels • Leading category management projects to optimise ranges and related merchandising • Creating forecasts for product demand to ensure sustainability of inventory • Managing budget development and revenue for the category • Developing strong working relationships with procurement, marketing and data management teams

• Lead a team of 8-10 individuals across the United States • Develop and maintain strong relationships with key stakeholders within the Home Depot and Lowe's Pro ecosystems • Implement strategies to support lead conversion and drive sales growth within the residential construction market • Identify and cultivate new growth opportunities within the residential construction Pro Market • Define and manage performance metrics for the team • Coordinate and deliver training programs for the team

• Design and maintain all qualified shipping lanes, both domestic and international. • Select and manage specialty couriers for cell and gene therapies. • Define appropriate temperature profiles, packaging configurations, and routing guides for shipments. • Establish contingency lanes for countries or timelines considered high risk. • Coordinate bulk shipments between manufacturing, packaging, and depot locations. • Ensure proper transfer of custody and real-time visibility of shipments. • Reconcile shipment and receipt acknowledgements, addressing any discrepancies. • Monitor and track shipments to all Adverum facilities and partners to ensure smooth transit through the logistical path, including international shipping. • Prepare all supporting customs documents for international shipments. • Maintain collaborative relationships with third-party vendors to ensure all shipping activities are connected with operations and compliant with quality requirements. • Record, coordinate, and oversee sample transfers between storage facilities to maintain chain-of-custody audit trails. • Document and maintain inventory and organization of all applicable materials including devices, products, components, consumables, and chemicals. • Accurately pull and issue material to support Manufacturing, Quality, and R&D needs. • Support technical and impact assessments for out-of-specification (OOS) temperature or humidity conditions occurring during storage and shipment of materials. • Manage country-specific import and export documentation. • Coordinate with brokers for customs clearances. • Maintain Harmonized Tariff Schedule (HTS) codes, commercial invoices, and necessary permits. • Anticipate and mitigate customs delays for clinical materials. • Monitor shipments for temperature excursions using data loggers. • Lead investigations and coordinate quarantine and Quality Assurance (QA) notifications. • Document deviations and support impact assessments. • Implement corrective actions when necessary. • Oversee and ensure quality of couriers, freight forwarders, and brokers. • Track performance metrics of all vendors. • Review Statements of Work (SOW), rates, and service level agreements. • Serve as the escalation point for shipment delays, lost shipments, or routing errors. • Communicate with sites, depots, QA, and clinical teams during logistics events. • Develop Standard Operating Procedures (SOPs) and lane qualification documents. • Standardize shipping documentation across operations. • Maintain risk assessments for all shipping activities. • Lead lessons learned efforts from shipment deviations and customs issues. • Ensure logistics documentation is audit and inspection ready. • Maintain chain of custody records and shipment trackers/logs. • Ensure all activities comply with Adverum Biotechnology’s standards and all applicable regulatory requirements, including FDA, EU, USDA, DEA, and DOT as applicable. • Manage the shipping tracker to ensure it contains the most up-to-date information for internal and external stakeholders.

• Lead IRT strategy during protocol development and study start-up. • Translate protocol requirements into IRT functional specifications in collaboration with functional leads. • Partner with Clinical Supply Chain to define inventory strategy within IRT, including buffer, overage, resupply thresholds, and expiry management. • Ensure packaging configuration is accurately reflected in the IRT system. • Own and govern all IRT enhancements and system request changes after go-live. • Assess the operational, site, and supply chain impact of proposed changes. • Act as a cross-functional impact assessor between Clinical Team, Supply Chain, QA, and IRT vendor. • Create and maintain a data change or systems change requests log and governance model to ensure inspection readiness. • Serve as the primary liaison with the IRT vendor. • Review and approve all necessary specifications with the internal team. • Lead User Acceptance Testing (UAT) and validation activities in partnership with Quality Assurance. • Govern change orders and mid-study updates. • Manage all IRT manuals with vendors and ensure effective rollout to study teams. • Monitor live study IRT performance. • Troubleshoot IRT-driven shipment and inventory issues, and collaborate with the vendor for resolution. • Act as the escalation point for site issues related to IRT. • Initiate deviations and/or CAPAs as required. • Prevent protocol deviations and missed dosing due to IRT misunderstandings or misalignments. • Align Clinical Operations, Clinical Supply Chain, Biostatistics, Data Management, and Clinical Development teams on IRT design. • Manage IRT training. • Establish an IRT governance model and best practices across trials. • Utilize data analytics tools to monitor supply chain performance and identify improvement areas. • Ensure IRT documentation supports FDA/EMA inspection readiness. • Maintain audit trails, validation documentation, and SOP alignment. • Ensure compliance with all relevant regulations and standards related to supply chain operations, including GMP and FDA requirements. • Identify potential risks within the supply chain and develop mitigation strategies. • Perform other job-related duties as assigned by management, within the reasonable scope of this position.