Job Description: • Provide scientific and strategic leadership for pharmacovigilance activities supporting Kite’s investigational and marketed products • Serve as lead author for complex aggregate safety reports, including PSURs, PBRERs, and DSURs • Author and review high-impact safety documents supporting regulatory submissions and lifecycle management • Lead safety reviews, including design of search strategies, data evaluation methodologies, and scientific interpretation of individual and aggregate safety data • Review individual case safety reports to identify and assess potential safety signals • Prepare and lead responses to safety-related requests from global health authorities • Serve as Pharmacovigilance Science Safety Lead for products in development • Ensure compliance with global regulations and internal procedures Requirements: • MD with 0+ years of relevant experience OR Doctorate with 2+ years of relevant experience OR Master’s degree with 6+ years of relevant experience OR Bachelor’s degree with 8+ years of relevant experience • 5+ years of direct pharmacovigilance experience performing aggregate reporting, safety analysis, and regulatory support activities • Strong knowledge of FDA, EMA, and ICH safety reporting regulations and GVP guidelines • Experience working with safety databases and tools, including Argus, Rave, MedDRA, and WHO Drug • Demonstrated ability to independently lead complex safety deliverables and make sound scientific judgments • Excellent written and verbal communication skills, with strong medical writing capability • Proven ability to collaborate effectively across functions and cultures and to lead within matrixed project teams Benefits: • Health insurance • 401(k) matching • Paid time off • Discretionary annual bonus • Discretionary stock-based long-term incentives Apply tot his job