Associate Director, Clinical Regulatory Writing - Hybrid Job at AstraZeneca in B

A global biopharmaceutical company is seeking a Clinical Regulatory Writing Manager (Associate Director) in Boston for a hybrid role. You will manage clinical regulatory writing activities and author critical documents to support drug development. Ideal candidates have a BS in Life Sciences and extensive medical writing experience in the pharmaceutical field. This position offers a competitive salary and comprehensive benefits, requiring a minimum of 3 days onsite weekly. #J-18808-Ljbffr