Associate Director, Clinical Supply Chain

Revolution Medicines, Inc.; California; On-site; USD 186,000 - 233,000; Full time

Job summary

Revolution Medicines, Inc. seeks a Clinical Supply Lead within the Pharmaceutical Development and Manufacturing organization to plan and deliver clinical supplies for oncology programs.

The role emphasizes supply planning, demand forecasting, packaging, labeling, distribution, and cold chain management. Responsibilities include authoring and reviewing technical documents (protocols, labels, IND/IMPD/NDA) and overseeing vendor selection and management; preferred background includes global Phase 3

Qualifications

• B.S./M.S. in scientific fields with 8+ years in clinical supply chain and logistics.
• Knowledge of pharma manufacturing, import/export laws and GxP standards.
• Experience with planning, packaging, labeling, distribution and cold chain.

Responsibilities

• Develop and deliver clinical supply plans for oncology programs.
• Manage demand forecasting, packaging, labeling, distribution and cold chain.
• Author and review technical documents (protocols, labels, IND/IMPD/NDA).
• Oversee vendor selection and management.

Skills

Clinical supply chain

Regulatory documentation

Team leadership

Global Phase 3 trials experience

Demand forecasting

Packaging & labeling

Cold chain management

Education

B.S./M.S. in scientific fields

Job description

Role: Clinical Supply Lead within the Pharmaceutical Development and Manufacturing organization, responsible for planning and delivering clinical supplies for RevMed’s oncology clinical programs. Responsibilities include developing supply plans, managing supply chain activities (demand forecasting, packaging, labeling, distribution, cold chain), authoring and reviewing technical documents (protocols, labels, IND/IMPD/NDA), and overseeing vendor selection and management. Requirements: B.S./M.S. in scientific fields with 8+ years in clinical supply chain and logistics, knowledge of pharma manufacturing and import export laws and GxP standards. Preferred: experience managing global Phase 3 oncology trials and team leadership. HighValue: oncology, clinical supplies, Phase 3, global logistics, regulatory documentation, cold chain management. WorkSetup: onsite Redwood City, CA, with salary range $186k–$233k.