Regulatory professional with specialized expertise in clinical research and regulatory start-up activities within the CRO setting. I bring a deep understanding of ICH-GCP regulations, IRB submissions, and regulatory compliance, ensuring the highest ethical standards are met across all phases of clinical trials. My experience spans managing multiple trials simultaneously, maintaining seamless communication between sponsors and study sites, and driving projects to successful completion.Therapeutic Areas:Cardiology Psychiatry (Schizophrenia, Postpartum Depression)Neurology (Spinal Muscular Atrophy) - pediatric trialInfectious Disease (COVID-19)In Vitro Diagnostics (IVD)Hepatology, Nephrology, Proteins, MetabolismI am passionate about advancing clinical research and playing a pivotal role in shaping the future of medicine to improve lives across the globe.