Senior Safety Scientist II

Role: Senior Safety Scientist supporting global patient safety and pharmacovigilance for Revolution Medicines' oncology portfolio, including early and late-phase clinical trials of RAS(ON) inhibitors. Responsibilities: lead safety surveillance, review and author safety documentation (protocols, IBs, ICFs, DSURs), perform signal detection and risk management activities, contribute to regulatory submissions, and ensure compliance with GVP and GCP standards. Serve as an active cross-functional team member, develop safety strategies, and maintain safety-related communication for clinical and regulatory purposes. Requirements: postgraduate qualification (MD, PharmD, PhD, MSc), 5+ years drug development experience with at least 3 years in drug safety, strong understanding of safety science, PV, and clinical risk management, excellent communication, and stakeholder collaboration skills. HighValue: oncology (RAS pathway), targeted therapies, clinical development, safety surveillance, regulatory documentation, global PV operations. WorkSetup: based in Redwood City, CA, with a salary range of $186K-$233K; specific work arrangement not specified but on-site presence indicated.