Sharmin Savaloni is a Global Clinical Trial Regulatory Lead at Roche with over 5 years of experience in the clinical research and pharmaceutical industry. They have extensive knowledge in leading global clinical trial application submissions to Health Authorities and provide strategic and technical advice on regulatory requirements, particularly in the EU CTR landscape. Sharmin's previous roles include Senior Country Approval Specialist and Regulatory Submissions Coordinator at PPD and Medpace, respectively, and they have gained experience as an intern at NeemCo Limited. They hold a Master of Science in Clinical Trials and Stratified Medicine, as well as a Master's in Drug Design and Discovery with Distinction, both from the University of Glasgow and the University of the West of Scotland.
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