Revolution Medicines is dedicated to discovering, developing, and delivering innovative targeted medicines for cancer patients. The company focuses on RAS-addicted cancers, which represent 30 percent of new human cancer diagnoses. Revolutionaries work tirelessly to develop cutting-edge therapeutic approaches, setting them apart in the industry with their commitment to tackling some of the toughest cancers.
Open Positions
Director, Regulatory Affairs
12+ years of experience in pharmaceutical/biotech industry or relevant work experience, 8+ years in Regulatory Affairs, strong track record in alliance management
Associate Director, Regulatory Affairs
7+ years of experience in the pharmaceutical/biotech industry or relevant work experience, with a minimum of 5 years in Regulatory Affairs. Strong working knowledge of US FDA and EU EMA Pharmaceutical regulations and guidance
Scientist II, Cancer Pharmacology, Translational Research
Ph.D. with quantitative science background, 2+ years of experience in cancer drug discovery and development, and strong theoretical understanding of PK/PD modeling
Vice President, Head of Global Medical Affairs Strategy
10 years experience in academic medicine, biotech and/or pharmaceutical industry, with a strong scientific background in oncology, excellent communication skills, and experience in building and leading a high-performing team
Director, Project Management – IEP & HEOR
15+ years of experience in biotechnology or pharmaceutical industry, 8+ years of direct project/program management in Medical Affairs or Evidence Generation, deep knowledge of HEOR, RWE, and medical affairs data generation practices and compliance frameworks
Senior Clinical Data Manager
Bachelor’s degree in health sciences, at least 5 years of Data Management experience, and solid knowledge of clinical data management principles
Director, Global Patient Safety Science
8+ years of drug development experience, 4+ years of Safety Science experience, postgraduate qualification
Associate Director, Clinical Pharmacology
Ph.D. or Pharm.D. with 5+ years of experience in Clinical and Quantitative pharmacology, expertise in clinical pharmacology and modeling, and a track record of applying modeling and simulation methodologies
Director, Clinical Quality
Bachelor's degree in a scientific or technical discipline and 15 years of experience in pharmaceutical clinical quality assurance
Vice President, Head of United States (U.S.) Medical Affairs
Advanced scientific degree (MD, PhD, or PharmD) with a specialization in oncology and at least 10 years of experience in Medical Affairs within oncology
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