David Ross
AstraZeneca, United States
Senior Director, Regulatory Data and Submissions
David Ross has led enterprise projects at AstraZeneca and Abbott Labs. He implemented enterprise solutions at AZ for cross-functional CSR Initiative, led the PQ/CMC pilot for AZ, developed roles for Early Clinical Authoring and leads Clinical Study Start up improvements in alignment with EU CTR 2022. He has delivered strategic and process improvements in labelling, CMC and Non-Clinical. He led the first eCTD Implementation in AZ. He is AZ representative of the PhRMA Regulatory IT Knowledge Group. He leads the GSO IRISS IRISS Forum, and is the AZ PhRMA IT group representative. He holds a B.SC in Biochemistry and a BASc. in Chemical Engineering. His graduate degrees include an MBA and Engineering Management from University of Ottawa.
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