Identify regulatory requirements related to the product and implement best practices for monitoring, interpreting, and communicating changes to internal teams. Proactively monitor, investigate, interpret, and communicate changes to regulatory requirements that may impact the current product. Work directly with product management to translate regulatory requirements into Veeva’s framework for use within our suite of applications.

Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Demonstrates the ability to combine knowledge of scientific, regulatory & business issues to enable development and commercialization of products that are developed, manufactured, or distributed to meet relevant US and Canada regulatory requirements. Assures that regulatory strategies defined within the GRPT are effectively implemented and maintained in line with changing regulatory and business needs. Supports products within the Oncology TA.