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 personnel
- Maintain Lilly's regional pharmacovigilance system across affiliates
- Oversee adverse event management and regulatory reporting activities
- Monitor quality metrics,



investigate gaps, and drive CAPAs
- Represent pharmacovigilance expertise in decision-making forums

Requirements:

- Bachelor's degree or higher in a relevant field
- Minimum five years of pharmaceutical industry pharmacovigilance experience
- Experience leading teams across affiliates or geographies
- Regulatory agency inspection experience
- Ability to travel as needed, approximately twenty percent

Apply regional leadership, regulatory knowledge, and quality expertise to strengthen pharmacovigilance execution across Lilly affiliates.

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