Senior VP, Regulatory Counsel - Infectious Disease & Vaccines

Eli Lilly and Company; Washington (District of Columbia); Hybrid; USD 234,000 - 343,000; Full time

Benefits offered by this job

401(k) plan

Medical, dental, vision benefits

Pension and vacation benefits

Job summary

Lilly is seeking an Associate Vice President, Assistant General Counsel for Infectious Disease & Vaccines Regulatory Legal. The role leads regulatory strategy across the vaccines portfolio and partners with global teams to manage development, registration, and post-market activities.

Ideal candidates have JD, US licensure, 7–10 years in regulatory matters, and in-house or regulatory agency experience in vaccines. Hybrid/remote options are possible; travel may be required.

Qualifications

• Bachelor's Degree and law degree (JD or equivalent) eligible to practice in the US
• Licensed to practice law in one of the 50 US states
• 7–10 years of legal experience with biologics regulatory matters
• In-house or regulatory agency experience in vaccine development or commercialization
• Authorized to work in the United States full-time

Responsibilities

• Lead regulatory legal strategy for vaccines and infectious disease globally.
• Provide governance and strategic guidance across development through post-market stages.
• Collaborate with Clinical Development, Regulatory Affairs, Manufacturing & Quality, Patient Safety and Policy.
• Develop governance models and external counsel strategy to scale the portfolio.

Skills

Regulatory leadership

Vaccine regulatory knowledge

In-house counsel experience

Cross-functional collaboration

Education

Bachelor's Degree + JD or equivalent

Job description

Lilly is seeking an Associate Vice President, Assistant General Counsel for Infectious Disease & Vaccines Regulatory Legal. The role leads regulatory strategy across the vaccines portfolio and partners with global teams to manage development, registration, and post-market activities.

Ideal candidates have JD, US licensure, 7–10 years in regulatory matters, and in-house or regulatory agency experience in vaccines. Hybrid/remote options are possible; travel may be required.