About the job
Revolution Medicines is a pioneering clinical-stage precision oncology company dedicated to the development of innovative targeted therapies aimed at inhibiting key targets in RAS-addicted cancers. Our R&D pipeline features RAS(ON) Inhibitors that are designed to suppress various oncogenic variants of RAS proteins, along with RAS Companion Inhibitors for combination treatment strategies. By joining Revolution Medicines, you will be part of a passionate team committed to transforming the lives of patients battling cancers with RAS signaling pathway mutations.
The Opportunity:
We are seeking a highly skilled and detail-oriented Senior Clinical Supply Chain Specialist to independently manage global clinical supply chain operations across multiple studies. This position is perfect for a proactive professional who excels in a fast-paced environment and can effectively oversee study-level supply planning, execution, and vendor coordination with minimal supervision.
Independently manage clinical supply chain activities for assigned studies, including planning, execution, and reconciliation.
Facilitate global depot and site distribution, coordinating Qualified Person (QP) release, import/export logistics, and temperature-controlled shipments.
Lead clinical label design, packaging, and labeling activities in collaboration with internal teams and external vendors.
Act as the primary point of contact for Contract Manufacturing Organizations (CMOs), depots, and Interactive Response Technology (IRT) vendors for assigned studies.
Develop and maintain study-level supply plans and forecasts, adjusting for protocol amendments, enrollment trends, and country/site activation.
Manage IRT system setup and maintenance, including drug assignment logic, inventory thresholds, and expiry management.
Monitor and manage Investigational Product (IP) inventory across depots and sites to ensure timely resupply and minimize waste.
Track and address temperature excursions, deviations, and other supply-related issues in collaboration with Quality Assurance (QA) and vendors.
Maintain study and depot-level accountability and reconciliation documentation to support regulatory compliance and study closeout.
Collaborate cross-functionally with Clinical Operations, QA, Regulatory, and Project Management to ensure alignment and timely execution.
Archive documentation on Trial Master Files as required.

