Description

You will plan, source, make, and deliver clinical supplies to support Revolution Medicines' clinical development programs, collaborating with cross-functional teams to ensure on-time, compliant supply for oncology trials.

Requirements

• B.Sc. or M.Sc. in scientific field with 5+ years pharmaceutical supply chain experience
• Knowledge of import/export laws, GMP, GDP, and end-to-end pharmaceutical supply chain
• Understanding of small molecule drug development and commercialization
• Strong project management and problem-solving skills
• Experience with global phase 3 oncology clinical trials preferred

Responsibilities

• Serve as clinical supply lead for assigned studies, developing and managing supply plans
• Plan, source, make, and deliver on-time, compliant clinical supplies
• Collaborate with Clinical Operations, QA, Regulatory, and PDM functions
• Manage clinical supply and logistics including forecasting, IRT, labeling, packaging, distribution, and inventory
• Author, review, or approve clinical and technical documents (e.g., batch records, protocols, regulatory submissions)