Senior Safety Scientist II

Role: Senior Safety Scientist supporting global oncology portfolio, focusing on safety science and pharmacovigilance across preclinical and clinical development stages. Responsibilities include safety oversight of clinical trials, review and authoring of protocols, Investigator's Brochures, ICFs, DSURs, and safety data summaries; conduct safety signal detection, risk management, and safety review of clinical data; contribute to regulatory safety documentation and responses. Maintain understanding of product safety profiles, support safety-related regulatory filings, and collaborate with cross-functional teams such as clinical, regulatory, and external vendors. Requirements: postgraduate qualification (MD, PharmD, PhD, MSc); 5+ years drug development experience with minimum 3 years in drug safety; strong knowledge of pharmacovigilance, GxP, GCP, and risk management; proven ability to influence and communicate effectively. Preferred: experience in oncology, biologics, or RAS-targeted therapies. High-Value: oncology, safety science, pharmacovigilance, clinical trial safety, regulatory safety documentation, cross-functional collaboration; location in Redwood City, CA, with a salary range of $186,000-$233,000. Work setup: on-site; no specific travel requirements mentioned.