Diverse Minds. Bold Disruptors. Meaningful Impact.
At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue extraordinary medicines in new ways, combining our people's exceptional skills with those of people from all over the globe.
We are hiring for an Associate Principal/Associate Director Clinical Regulatory Medical Writer/Submission Lead! In this role, you will be channeling our scientific capabilities to make a positive impact on changing patients' lives. You will help drive late-stage development of our innovative pipeline, redefining exciting science into valued new medicines, and ensuring patients around the world can access them.
Are you ready for an exciting, strategic position in clinical regulatory medical writing?
Working in our Global Medicines Development organization, you will be leading the way for the communication of clinical submissions for marketing approval (NDAs/BLAs/MAAs), redefining our exciting pipeline of novel small and large molecules into valued new medicines in oncology, respiratory and cardiovascular indications. Join us at one of our worldwide research bases in Gaithersburg, MD and thrive in our scientific excellence and collaboration. Be a part on an extraordinary team of Medical Communication Scientists - our group has an outstanding record of efficiently driving crucial communications excellence in project teams to achieve successful submissions and approvals!
Main Duties and Responsibilities-
Build and Deliver Clinical-Regulatory Submissions:
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