Lilly in Indianapolis is seeking a Global Regulatory Lead to drive global regulatory strategies from development through lifecycle. You will lead a cross-functional team, oversee US FDA submissions, and shape interactions with health authorities to support registration goals. The role requires 8+ years in regulatory affairs or drug development, with an advanced degree preferred. Travel 10–15% and relocation to Indianapolis is provided.

Also on the board Same function, level within a rung

Level

Manager

Location

Indianapolis, IN

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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