Descripción de la oferta
We are partnering with a leading biopharma company to identify a Clinical Supply Chain Manager to oversee global clinical trial supply operations. This critical role ensures uninterrupted availability of investigational products, comparators, and ancillary materials across Phase I–III studies. You will collaborate closely with Clinical Operations, CMC, Regulatory, Quality, CMOs/CDMOs, depots, and logistics partners to drive efficient planning, inventory management, distribution, and compliance. ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación.Key Responsibilities: Lead end-to-end clinical supply planning, including forecasting, packaging, labelling, distribution, and returns Manage relationships with CMOs, depots, and logistics providers Monitor inventory, mitigate supply risks, and ensure GMP/GDP/GCP compliance Support IND/CTA submissions with supply documentation Oversee IRT supply strategy and contingency planning Track budgets and key supply metrics (OTIF, waste, expiry) Qualifications: Bachelor’s or Master’s in Supply Chain, Life Sciences, Engineering, or related field 5–10+ years’ experience xcskxlj in clinical supply chain within pharma or biotech Experience with global Phase II/III trials preferred Strong knowledge of GMP, GDP, GCP, and regulatory requirements Experience with CMOs/CDMOs and global distribution networks Familiarity with IRT systems and clinical planning tools If this role seems interesting, please send a copy of your CV to
