Overall work experience of 16.6 years in Clinical Data Management, Product Management, Project Management and People Management.  Experience in ‘End-to-End activities’ for Phase I-IV studies, handling start-up, conduct and close out activities including CRF designing and medical coding.  Lead Data Manager. Study Oversight lead for different studies.  Part of Staff development team which is responsible for coaching responsibilities, template review work, process updates and improvements, training needs, internal process, and documentation updates, etc.  Led the team of 6 CRF designers and Medical coders  Part of QC team. SPOC for the sponsor CDM Audit.  Exposure to CDISC standards  Therapeutic areas: Endocrinology, Autoimmune, Neurology, Cardiovascular, Nephrology, Oncology. Certified scrum master