Emma Kent is an experienced clinical trials professional with a background in managing oncology clinical trials and coordinating research initiatives within prestigious institutions. At UCL, Emma coordinated phase 3 clinical trials adhering to ICH-GCP standards and produced essential trial documentation. Following a role at King's College London as a Clinical Research Coordinator, Emma served as Senior Manager at NICE, overseeing the implementation of Managed Access Agreements across various disease areas. Currently, as a Policy, Value & Access Partner at Roche, Emma continues to leverage expertise in evidence generation. Emma holds a Bachelor of Science in Immunology from the University of Bristol.
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