Teams at Novartis

Leads the global expansion of Inclusive Health Accelerators across priority markets, partnering with country and cross-functional teams to identify healthcare access barriers and scale sustainable solutions. The role develops methodologies, partnerships, implementation roadmaps, governance, KPIs, dashboards, and learning systems; integrates inclusive access priorities into business and market planning; and translates data, community insights, and market context into measurable improvements for underreached populations.

Manages pharmaceutical product registrations, regulatory submissions, approvals, licensing, variations, renewals, safety communications, and post-approval activities. Develops registration strategies, supports clinical trial approvals and product launches, maintains regulatory databases, monitors compliance with pharmaceutical regulations and industry codes, and coordinates with health authorities and cross-functional stakeholders. Also supports adverse event and technical complaint reporting.

Manages end-to-end clinical trial supply activities, including demand planning, packaging, labeling, randomization, distribution, warehousing, resupply, risk mitigation, budgeting, and regulatory compliance. Advises clinical trial teams on supply strategy, develops project plans, coordinates cross-functional stakeholders, and ensures continuity of investigational medicinal products across participating countries.