Director - Regulatory Affairs Resource, Analytics and Insights Lead

Role: The position is within Gilead's Regulatory Affairs Business Operations, focusing on RA Human Capital. Responsibilities include managing end-to-end resource planning, data quality, and infrastructure to support strategic workforce decisions, demand-supply balancing, and capacity optimization across Regulatory Affairs. The role involves leading special projects, collaborating on workforce planning, and influencing culture around resource management practices, with an emphasis on continuous improvement and operational excellence. Requirements: MA/MS/MPH with 10+ years in Regulatory Affairs or project management, or PhD with relevant experience, or BA/BS with 12+ years in similar roles. Strong expertise in resource forecasting tools such as Planisware and Smartsheet, with knowledge of drug development lifecycle processes, is essential. Preferred skills include experience in performance management, business process excellence, change management, and stakeholder influence in a highly matrixed environment. High-value specifics: focus on regulatory lifecycle management, resource modeling, and cross-functional collaboration within a global biopharma setting. Leadership responsibilities include developing talent, fostering inclusion, and driving team empowerment. The role may involve travel as needed. Location flexible within the US, with salary range approximately $191,250 to $272,250, plus benefits and incentives.