AstraZeneca plc in Barcelona is seeking an Associate Director/Director, Clinical Regulatory Writing to lead pivotal CVRM submission content and strategy. You will mentor teams, shape submissions from development through approval, and drive best-in-class regulatory communications with senior stakeholders.
You will guide cross-functional authoring groups, ensuring regulatory compliance, quality, and timely delivery across complex programs while aligning with product strategy.
📌 Director, Clinical Regulatory Writing — Strategy (Distrito del Ensanche)
🏢 Astra Zeneca
📍 Distrito del Ensanche
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