Senior Manager, Global Patient Safety Operations

Role: Manage and oversee global patient safety operations in clinical oncology programs focused on RAS-targeted therapies, ensuring compliance with regulatory requirements. Responsibilities: lead safety information collection and reporting, collaborate with cross-functional teams, oversee PV CROs, ensure timely safety submissions to authorities, support safety data management, and contribute to protocol and safety document authoring. May supervise junior team members. Requirements: Bachelor's in healthcare; 5+ years in pharmacovigilance operations, with hands-on experience managing CRO/vendor relationships, safety compliance, and global safety regulations in clinical trials. Preferred qualifications include a Master’s degree and 7+ years of PV experience, especially with investigator-sponsored trials and extended use programs. HighValue: oncology, targeted therapies (RAS inhibitors), clinical development, pharmacovigilance, safety data management, global regulatory compliance, cross-functional collaboration. WorkSetup: likely onsite in Redwood City, CA, with a salary range of $164,000–$205,000, plus benefits.