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Leads cross-functional teams in the planning and execution of clinical trials in oncology, ensuring quality, timing, and budget adherence.

This position involves overseeing CMC regulatory affairs from development through post-marketing, including document creation for clinical trials and drug approvals.

As Associate Director in SPE, you will lead engineering teams to design scalable enterprise-grade platforms. Responsibilities include technical leadership, mentorship, and driving innovation while ensuring efficiency in project delivery and collaboration across teams.

The Product Manager will define and articulate the product vision, manage user needs, ensure compliance, and lead scalable solutions focusing on AI and innovative technologies at Lilly.

The Associate Director PRA at Lilly will drive the access strategy for medicines, manage hospital operations, and build relationships with stakeholders to ensure pricing and access goals are met, while supervising the PRA team.

The SecOps Engineer ensures secure access to enterprise resources by managing IAM systems, incident responses, and system performance, while enhancing the IAM program and collaborating with IT teams.

The Principal Process Engineer leads process knowledge development, tech transfers, and continuous improvement in API manufacturing, ensuring safety, quality, and operational excellence.

Lead AI/ML strategy for oncology discovery, innovate data integration platforms, advance computational design, oversee experiments, and mentor a high-performing team.

The role involves leading drug substance manufacturing, overseeing technical issues, managing scientists, and ensuring compliance with regulations. Requires expertise in peptide chemistry and manufacturing processes.

The Sr. Director of Parenteral Engineering leads strategic projects, operational excellence, and effective communication across manufacturing sites while ensuring safety and quality.