Join us at AstraZeneca, where we are using cell therapy to revolutionize the treatment of life-threatening immune-mediated diseases. Our exceptional team is working on the groundbreaking area of cellular therapies, and we are investing in internal capabilities to discover and accelerate the delivery of next-generation cellular therapies for patients. As part of our Clinical Regulatory Writing team, you will play a crucial role in bringing these transformative therapies from the lab to life.
We are now recruiting a Director, Clinical Regulatory Writing (CReW), Immunology Cell Therapy Program Lead. In this role you will provide expert leadership to the delivery of the product pipeline through partnering with senior leaders to define and lead the global communications strategy. You will be a leader for clinical regulatory writing activities within the disease area for cross functional teams and external vendor partners.
This opportunity is available at our Boston Seaport, MA (USA) location.
We expect employees to be on-site for a minimum of three days per week and are therefore unable to offer remote-based working.
The Director, CReW, develops communications strategies to guide programs while advocating and developing best practices for document and accelerated submission delivery, represents strategic communications expertise in business process optimisation and improvement initiatives, and supports the growth and development of internal talent.
What You will Do
As a leader in CReW you will be expected to:
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