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I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have more than 17 years and 9 months of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 13 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I have experience with all aspects of data management including project management, edit check writing/reviewing, data locking, eCRF design, full life cycle of study management from Protocol Concept through Database lock. I have been responsible for management and delivery of several phase I-IV clinical trials across the globe thereby consistently handling and meeting the project timelines,Involved in end-to-end Clinical Data Management activities from start up to close out phase(e.g. Project Set up, eCRF Design, UAT, Mapping UAT, ) for various EDC trials. I am a self- starter and quick learner with willingness to learn new and innovative things and meeting the targets on scheduled time, excellent planning and organizational skills, able to manage multiple projects concurrently with the ability to maintain a consistently high standard of work and work ethics.Capable of problem solving, critical thinking,leadership and team work. I have successfully coordinated study team of high performing individuals. Attention to detail and quality and have experience of attending internal and external audits. My functional experience includes Understanding of clinical trial methodology, ICH GCP Guidelines and other guidelines, Good Clinical Data Management Practices,Clinical trials-phase I to phase IV, Drug development, Drug laws and Regulation, Business-development process and medical terminology. I Love training the Data Administration staff on Clinical electronic data capture systems. My therapeutic experience includes Oncology, Infection, Plaque psoriasis etc.