Lead the development of appropriate business-focused, high‑quality, timely regional regulatory strategy and its execution for assigned asset(s), consistent with relevant enterprise goals and respective product profile. This goal is achieved as a component of an overall global regulatory approach while ensuring compliance with both internal GSK process/policy and with regional regulatory requirements to deliver the best possible labeling in close collaboration and alignment with respective Global Regulatory Lead (GRL), Local Operating Company Regulatory Affairs (LOC RA) and Regional Medical & Commercial Leads.
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