Associate Director, Clinical Regulatory Writing - Hybrid Job at Astrazeneca in C

A leading pharmaceutical company is seeking an Associate Director for Clinical Regulatory Writing, responsible for managing writing activities and authoring complex regulatory documents in a hybrid setting. Candidates should possess a BS in Life Sciences and have over 7 years of experience in medical writing within the pharmaceutical industry. This role emphasizes strategic communication leadership, flexibility, and collaboration in drug development. #J-18808-Ljbffr