Senior Specialist, Clinical Supply Chain

Revolution Medicines•Redwood City, CA

13d•$120,000 - $150,000•Hybrid

About The Position

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Independently support global clinical supply chain operations across multiple studies. This role is ideal for a detail-oriented, proactive professional who thrives in a fast-paced environment and can manage study-level supply planning, execution, and vendor coordination with minimal oversight. Independently manage clinical supply chain activities for assigned studies, including planning, execution, and reconciliation. Support global depot and site distribution, including coordination of 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. Serve as the primary point of contact for CMOs, depots, and 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 IP inventory across depots and sites, ensuring timely resupply and minimizing waste. Track and resolve temperature excursions, deviations, and other supply-related issues in collaboration with 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.

Requirements

B.S. in a scientific or supply chain-related field.
3–6 years of experience in clinical supply chain and logistics.
Demonstrated experience supporting global clinical trials, including EU QP release and import/export logistics.
Strong working knowledge of IRT systems, clinical packaging/labeling, and temperature-controlled distribution.
Proficiency in Microsoft Excel.
Excellent organizational, communication, and problem-solving skills.
Ability to work independently while collaborating effectively across functions and with external partners.

Nice To Haves

Tableau and/or PowerBI experience is a plus.
Experience with oncology trials and complex study designs is a plus.
Clinical supply chain and logistics in a biotech or pharmaceutical environment.

Responsibilities

Independently manage clinical supply chain activities for assigned studies, including planning, execution, and reconciliation.
Support global depot and site distribution, including coordination of 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.
Serve as the primary point of contact for CMOs, depots, and 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 IP inventory across depots and sites, ensuring timely resupply and minimizing waste.
Track and resolve temperature excursions, deviations, and other supply-related issues in collaboration with 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.