Working with a high degree of independence, this role serves as the sponsor-side clinical supply representative on cross-functional study teams and translates protocol, enrollment, country, manufacturing, release, and regulatory assumptions into an executable supply strategy. Build and maintain integrated start-up plans with the team covering demand assumptions, manufacturing and release, packaging and labeling, IRT cross-configuration, depot activation, import/export readiness, site supply, comparator and ancillary sourcing, and contingency stock.