Initial Therapeutics, Inc.

Lilly seeks an experienced medical writer to lead planning, authoring, and review of complex clinical and regulatory documents across development programs, collaborating with clinical development, regulatory affairs, biostatistics, medical affairs, and legal to ensure scientific accuracy and regulatory compliance. The ideal candidate holds a bachelor’s degree in a scientific field (Master’s or PhD preferred) and at least eight years of medical writing experience in pharma/biotech/CRO, with #J-18808-Ljbffr

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Verve Therapeutics, a Lilly Research Labs subsidiary, is a clinical‑stage genetic medicines company on a mission to solve cardiovascular disease. Founded by leaders in cardiovascular medicine and gene editing, Verve is developing one‑time gene editing treatments aimed at turning chronic management into a single‑course cure. Its lead programs target...