Vishu C.
Regulatory Affairs & Study Start-up Manager @IQVIA
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WORK HISTORY
Regulatory Affairs & Study Start-up Manager @IQVIA
Provides regulatory oversight and lead on global clinical trials- Manages and executes the site identification process and performs regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements either at the global, regional, or country level - Prepares and manages site regulatory documentation- Reviews and negotiates site regulatory documents and contracts with sites and sponsors- Maintains, reviews, and reports on site performance metrics- Serves as the primary point of contact for investigative sites- Tracks completion of regulatory and contractual documents for sites- Ensures contracts are fully executed- Establishes project timelines
EDUCATION
UCL
Master's degree, Stroke Medicine
University of Toronto
Bachelor of Science - BS , Double Major in Neuroscience and Psychology
ABOUT VISHU C.
I’m a Regulatory Affairs & Study Start-Up Leader with 11+ years of global experience driving regulatory strategy and Phase trial activation across complex, multi-site programs.Experienced with leading cross-functional teams and optimizing start-up workflows, I bring structure, accountability, and strategic focus to high-growth environments.I’m driven by opportunities to strengthen regulatory infrastructure and support scalable, high-performing clinical operations.
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