• Manage drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical studies. • Actively develops and oversees supply plans to ensure accurate and continuous supply to patients while reducing risk and minimizing waste. • Represents Clinical Supply Chain to internal stakeholders and manages relationships with external supply partners. • Has a working knowledge of clinical supply best practices, IRT systems, as well as experience working within a cGMP environment. • Works with management to develop and implement process improvements to build the organization for the future.