14 oct
|
Astra Zeneca
|
Les
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.#J-18808-Ljbffr
📌 Director, Clinical Regulatory Writing — Strategy & Submissions (Les)
🏢 Astra Zeneca
📍 Les