Lalitha Goteti is an Associate Director specializing in Regulatory Medical Writing at Pfizer, where they currently serve as Submission Lead for Paxlovid. Previously, they held the position of Director in Regulatory Medical Writing at AstraZeneca and worked as a Senior Regulatory Documentation Scientist at Roche, where they led the authoring of critical regulatory documents. Lalitha's earlier roles included medical editing and writing for various organizations, and they earned a Master's degree in Biochemistry from Bangalore University. Their extensive experience underscores a commitment to excellence in regulatory content architecture.
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