Back to jobsPlanning, 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
Developing, reviewing, and approving SOPs and trial documentation in line with internal procedures and regulatory requirements
Serving as a subject‑matter expert in biological IMPs and temperature deviation management
Participating in and presenting at global Investigator and Monitor Meetings
Leading optimization and improvement projects to support Global Clinical Operations
