Position Overview
The Study Optimization Manager (SOM) role is accountable for the development, implementation and oversight of optimal clinical supply strategies using advanced modeling techniques and software for selected high-value clinical trials. This R&D enterprise responsibility impacts optimal design of clinical trials, acceleration of clinical supply, and oversight of strategic, enterprise-level risk mitigation and supply management.
Key Responsibilities:
Apply strategic, cross-program knowledge of clinical supplies to positively influence clinical trial design and supply chain decisions.Accountable for independent development and management of advanced demand and supply models in the N-Side Supply Application or other appropriate tools.Builds understanding of the business context, systems, environment, strategy and people assigned to the given area. This also includes an understanding of the relevant and complex internal and external high-volume data so...