Qualifications
Advanced degree (PhD, MD, or equivalent) in a relevant scientific discipline.Minimum of 10 years of experience in regulatory affairs, preferably in oncology.Demonstrated expertise in early development regulatory submissions and interactions with regulatory agencies.Strong leadership skills with a track record of managing high-performing teams.Excellent communication and interpersonal skills.Ability to thrive in a fast-paced, dynamic environment.
About the job
Revolution Medicines, Inc. is seeking a highly accomplished Senior Director to lead our Early Development Regulatory Affairs team. In this pivotal role, you will be responsible for shaping regulatory strategies for our innovative oncology programs, ensuring compliance with all regulatory requirements while advancing our mission to transform the lives of patients.
The ideal candidate will possess extensive experience in regulatory affairs within the pharmaceutical or biotechnology sectors, with a proven track record of successful submissions and interactions with health authorities. You will collaborate closely with cross-functional teams, including clinical, preclinical, and commercial, to drive our development efforts forward.
About Revolution Medicines, Inc.
At Revolution Medicines, we are committed to discovering and developing targeted therapies to treat cancer. Our innovative approach is defined by a deep understanding of the biology of cancer and a commitment to addressing the unmet needs of patients. Join us in our mission to revolutionize cancer treatment.