MD

Michael Davis

Director, Clinical Regulatory Writing

Michael Davis is currently the Associate Director of Clinical Regulatory Writing at AstraZeneca, where they leverage their expertise in digital transformation, regulatory compliance, and document management systems. They previously held roles as an Associate Professor at Blekinge Institute of Technology and as a Medical Writer at Oncopeptides AB, where they coordinated regulatory document preparations for submissions to international health authorities. Michael has a Ph.D. in English with a focus on Rhetoric from The University of Texas at Austin and is fluent in both English and Swedish. Throughout their career, they have demonstrated a strong commitment to enhancing communication and collaboration within global teams.

Location

Stockholm, Sweden

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