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Associate Director of Global Regulatory Affairs Project Management

Revolution MedicinesRedwood City, California, United States
On-site Full-time

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Experience Level

Senior Level Manager

Qualifications

Advanced degree in life sciences or related field; a PhD is preferred. A minimum of 7 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry. Proven track record of successfully managing regulatory submissions and interactions with health authorities. Strong understanding of regulatory requirements for drug development and commercialization. Excellent leadership, communication, and project management skills.

About the job

Revolution Medicines is seeking an experienced and strategic Associate Director of Global Regulatory Affairs Project Management. In this pivotal role, you will lead the planning and execution of regulatory activities for innovative therapeutics, ensuring compliance with global regulations while driving project success. You will collaborate closely with cross-functional teams to develop and implement regulatory strategies that align with our mission of transforming the lives of patients with cancer.

About Revolution Medicines

Revolution Medicines is at the forefront of developing transformative medicines for patients with cancer. Our innovative approach leverages cutting-edge science to identify and target the underlying mechanisms of disease, providing hope to patients who need it most. Join us in our mission to redefine cancer treatment and make a meaningful impact on patient lives.

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