Job Description

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...

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