Contributes to and executes against the RAPV strategy by creating 1-3 year plans for the RA system and process capabilities, aligning their group with the other RAPV Enablement groups, considering industry initiatives, Health Authority guidances, software vendor capabilities, corporate strategy, internal RA process improvements, system interactions with other functions and end user input. Identifies the need for and ensures the assimilation of detailed interpretive analyses of complex regulatory guidance documents, regulations, or directives that impact products and operations; prioritizes short- and long-term projects to implement relevant changes in system configurations and business processes to maximize efficiency and/or improve compliance.