Your role

As a Clinical Supply Manager, you will lead end‑to‑end clinical trial supply activities across global clinical studies.

Your key responsibilities include:

• Planning, coordinating, and managing clinical trial supply timelines in collaboration with internal teams and external partners


• Leading end‑to‑end clinical supply management including IMP, non‑IMP, comparator, and ancillary sourcing, forecasting, waste reduction, handling, and destruction


• Managing budgets, forecasts, RFPs, service requests, and approve study‑related invoices


• Overseeing labeling, packaging, distribution, import/export, and external packaging facilities in compliance with GMP, GDP, and GCP requirements


• Acting as IRT lead, responsible for system setup, execution, reconciliation, and close‑out


• Ensuring protocol consistency from a trial supplies perspective


• Develo...