• Study Manager (SM) is a key member of the Global Study Team contributing to delivering the clinical study to time, cost and quality, and ensuring inspection readiness by taking an oversight over study eTMF completeness. • SM works in close partnership with the Study Delivery Lead (SDL) on end-to-end operational study delivery activities, from study setup to study archival. • Focus on setting up, maintaining and ensuring completeness of internal systems / databases / tracking tools and project plans (CSAP). • Works cross-functionally, with internal and external partners, on clinical study management activities, for in-house and outsourced studies across all phases and therapeutic areas. • Responsible for monitoring study conduct and progress, identifying, resolving and escalating risks/issues which may impact delivery of the study to the necessary quality, timeline and budget objectives.

• Manager related duties to include following with wholesalers: weekly tracking vs budget, monthly Wholesaler Performance Reviews, daily/weekly/monthly communication on all Non-Alc related initiatives • Direct liaison from Non-Alc Corporate team to Region team • Trains wholesalers on all aspects of Non Alcoholic brands: Route to market, Non-Alc selling to retailers, pricing, Independent sell-in (Free Fills, Customer Market Agreement) • Recommends and implements Non-Alc sales strategies for improvement based on market research and competitive analyses. • Creates, presents, and tracks sales incentive programs to wholesalers. • Shares / creates best practices to drive Non-Alc growth. • Works with Non-Alc Key Account Managers for weekly follow up on Items Not Brought In Reports and other key gaps for each major chains & programs that are sold in. • Organizes and executes effective Market Blitz’s w/ Brewery Sales force. • Manages Regional Non-Alc annual budget, requesting incremental funds when necessary, and completing post-even analysis to determine ROI of various line items.

• Lead engagements end‑to‑end—from scoping and analysis through delivery—driving projects to completion. • Manage and develop junior team members; set milestones and ensure execution. • Communicate with clients throughout the engagement; present findings and deliverables in a clear, decision‑oriented, value‑adding way. • Perform and review complex financial analyses and economic/industry research. • Oversee preparation and quality of reports, exhibits, tables, and presentations across multiple models and assignments. • Contribute to practice development and process improvements.

• Lead the development of next-generation mobile, backend, and cloud-connected solutions for regulated medical devices and digital health products • Shape system architecture, review technical deliverables, and ensure that digital health products are secure, scalable, and compliant with regulatory expectations • Partner with internal teams and contract developers to plan, integrate, and deliver mobile, cloud, and device-connected digital solutions • Provide technical guidance to ensure products meet clinical, regulatory, cybersecurity, and business requirements • Manage architectural decisions, enforce lifecycle processes, and ensure consistent, high-quality execution across internal and outsourced contributors • Oversee outsourced development for mobile applications and backend services, ensuring alignment with SPR’s standards and regulatory needs • Collaborate with cybersecurity and development partners to embed security-by-design and privacy principles into software development • Strengthen SPR’s digital software development framework, templates, and toolchain