Associate Vice President- Assistant General Counsel, Infectious Disease & Vaccines, Regulatory Legal

Eli Lilly and Company

Washington (District of Columbia)

Vor Ort

USD 180.000 - 320.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Lilly seeks an Associate Vice President - Assistant General Counsel for Infectious Disease & Vaccines, Regulatory Legal. You will provide strategic legal counsel across the product lifecycle.

Collaborate with Clinical Development, Manufacturing, and Policy to shape regulatory pathways, engage health authorities, and drive portfolio integration and growth.

Qualifikationen

  • JD (US) or equivalent, licensed in one US state.
  • 7-10+ years of legal experience in biologics, vaccines, or regulatory law, with in-house or law firm experience supporting vaccine development or commercialization.

Aufgaben

  • Lead global regulatory legal strategy.
  • Support emerging therapeutic areas.
  • Manage interactions with health authorities.
  • Advise on regulatory pathways.
  • Build legal frameworks for portfolio integration and growth.

Kenntnisse

Regulatory law
Vaccine regulation
Strategic counsel

Ausbildung

JD (US)

Jobbeschreibung

Role

Associate Vice President - Assistant General Counsel, Infectious Disease & Vaccines, Regulatory Legal, providing strategic legal counsel for Lilly's infectious disease and vaccine portfolio across the product lifecycle.

Responsibilities
  • lead global regulatory legal strategy
  • support emerging therapeutic areas
  • manage interactions with health authorities
  • advise on regulatory pathways
  • build legal frameworks for portfolio integration and growth
Collaborates

Collaborate closely with cross-functional teams such as Clinical Development, Manufacturing, and Policy, ensuring compliance with biologics and vaccine-specific regulations.

Qualifications
  • JD (US) or equivalent, licensed in one US state, 7-10+ years of legal experience in biologics, vaccines, or regulatory law, with prior in-house or law firm experience supporting vaccine development or commercialization.
Preferred Skills
  • expertise in vaccine legal frameworks, clinical trial safety, biologics manufacturing, and global regulatory submissions.
High Value Areas

HighValue: vaccines, infectious diseases, biologics, regulatory strategy, global health authority engagement, portfolio lifecycle management, work setup in Indianapolis or Washington, DC, with 10-15% travel.

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