Assoc Director Safety Science

Role: Associate Director, Safety Science at Erasca, supporting safety and pharmacovigilance across oncology molecules in early and late-phase clinical development. Responsibilities: oversee signal detection and management activities, prepare safety documentation (e.g., DSUR, IND reports), review clinical protocols and safety data, contribute to safety assessments, and collaborate with safety operations and external vendors. Requirements: healthcare professional degree (MD, PharmD, RN), 4+ years in drug development with at least 2 years focused on drug safety, strong understanding of safety science, PV regulations (GVP, GCP), and clinical risk management. Preferred: experience with safety databases like Oracle Argus, leadership skills, and effective communication abilities. HighValue: oncology (cancer), immuno-oncology, precision oncology, molecular targeted therapies, regulatory safety reporting, cross-functional clinical trial team interface. WorkSetup: hybrid (San Diego or South San Francisco) or remote U.S.; no travel specified.