Lead regional pharmacovigilance operations at Lilly, applying quality systems and regulatory expertise across aligned affiliates and countries.As Associate Director or Director, you will translate global pharmacovigilance strategy into consistent regional execution. The work spans adverse event management, reporting, risk management, inspections, and Pharmacovigilance System Master File activities. You will connect affiliate safety teams with Global Patient Safety, Qualified Persons for Pharmacovigilance, and the Medical Quality Organization.Key Responsibilities: Lead, develop, and motivate regional pharmacovigilance personnelMaintain Lilly's regional pharmacovigilance system across affiliatesOversee adverse event management and regulatory reporting activitiesMonitor quality metrics,



investigate gaps, and drive CAPAsRepresent pharmacovigilance expertise in decision-making forumsRequirements: Bachelor's degree or higher in a relevant fieldMinimum five years of pharmaceutical industry pharmacovigilance experienceExperience leading teams across affiliates or geographiesRegulatory agency inspection experienceAbility to travel as needed, approximately twenty percentApply regional leadership, regulatory knowledge, and quality expertise to strengthen pharmacovigilance execution across Lilly affiliates.#J-18808-Ljbffr

📌 Regional Pharmacovigilance Director (LaSalle)
🏢 Eli Lilly
📍 LaSalle