About the role: Senior Clinical Data Associate -responsible for day-to-day data processing operations for data management projects, including CRF (or other study data document) tracking, entry, and filing. Provides administrative and project management support to CDMs
About the role: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs. Responsibilities Member
Company - Novo Nordisk Global Business Services (GBS) Department - Central Monitoring Unit Location - Bangalore, India Are you ready to shape the future of clinical trial oversight and drive medical data quality