Acting as Submission Lead with 6 years plus of experience with IQVIA Asia Pacific and Pfizer. I am currently working with GSK in Central Regulatory Affairs Team for Drug Development and Content delivery with additional roles of acting as a China Subject Matter expert, Process trainer, ROW Champion and have strong cultivated knowledge over the years with regards to ICF preparation, EDP review and submission for ROW, substantial Amendment to ANZ, Creating content plan for RA submissions and many more such affiliated tasks. I am looking for lucrative role that helps me learn more in the field of Core Regulatory. My knowledge and training will help me, my team and the company to grow and contribute together towards the betterment of patients/subjects quality of life and future Market value with an effort to improve public health. I am very passionate towards my career and very eager to learn more in this field.I have sound knowledge in the below TMF system:WingspanIntelligent TMF (iTMF)ELVISRSU-WFCTMSSAWTrained in InfostartVeeva Vault (Reg and Clinical Vault)Been a Delegate at Global Pharma Regulatory Summit and also Represented GSK as a guest lecturer for universities in India