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