Om Bichewar

Background

About Om Bichewar

A proactive Life Science IT professional holds M. Pharm qualification with 14+ years of work experience & proven track record of stakeholder management, skilled in gathering business requirements, and providing Digital, Med Tech, and Therapeutic solutions as per their Business needs. Expertise in Commercial Landscape of Life sciences in area such as, Contracts & Tendering, Global Price Management, Global Market Access, Product Launch, Business Intelligence, B2B Sales, Business Development, KOL Development, Medical devices consultant & Medical Science Liaison. Profound understanding and Experience in Software Development Life Cycle (SDLC) as Senior Business Analyst and Domain Expert/ SME for Pharma and Medical Devices Clients. Certified SAFe Agilist Professional, Experienced in Agile Methodology & work with Scrum Master for executing Scrum ceremonies such as Backlog Refinement, Sprint Planning, Stand Up, Sprint Review & Sprint Retrospective. Delivered strategic leadership & consulting Life Sciences projects with changing priorities, ensuring focus on quality, timeliness and continuous Business Process Improvement. Executed Interactive Data Products for Market Access & Pricing team for Pharma client using BI tools. Executed BI Projects by Integrating with Relational Databases & other Systems such as Oracle, Redshift, Amazon S3, Apache Hive, Veeva CRM, & Dremio. Accelerated the success of organizations by bridging the gap between Healthcare Professional & Pharmaceutical/Medical Devices Organizations. Well versed with Regulatory Compliance such 21 CFR,(Part 11, Part 50, Part 210, and Part 211), HTA Submission, GxP (GCP, GMP, GVP, and GMLP) HIPPA/HITECH, Medical Devices Regulation (MDR), ISO 13845 and 14155 standards, EMR, HL7, ICD, Pharmacovigilance, US Healthcare (Medicare/Medicaid) and USFDA Regulatory submissions. My domain expertise include Clinical trials, Regulatory affairs, Market Access & Pricing, Medical device consulting, & Pharma commercial Operations.