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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Medical / Healthcare |
| Functional Area | Allied Health Services |
| EmploymentType | Full-time |
1. Review Global Documents (e.g., GGDs) based on available evidence (e.g., Core Data Sheet, medical literature, data on file) ensuring comprehensive, high quality, scientifically correct and consistent medical information. Closely interact with the GMA Brand team and ensure review, approval and availability of documents in the global Novartis medical information database 2. Accountable for managing all compound-related queries including development, editing, and approval of responses to medical enquiries, by obtaining information from internal sources (e.g., safety, regulatory, development, research) and published materials. Adhere to requirements of the Risk Management Plan (RMP) and support the adverse events (AE) and product complaints (PC) handling process. 3. Manage Novartis medical information system and database, including literature library. Manage timely update for all assigned products in collaboration with medical affairs and development teams. Accountable for medical information global database accuracy and completeness. Train users and oversee user access within the assigned therapy area. 4. Develop, disseminate, and manage internal Med Info related news flow of key product and disease information on an on-going basis 5. Responsible for medical information and communication responsibilities, e.g. escalated enquiry management, to meet Regional, CPO, and Franchise needs while fostering optimal use of Novartis products. 6. Maintain processes to optimize communication and exchange across the Franchises, Regions, CPOs, and medical affairs. 7. Responsible for collection and reporting of relevant metrics/KPIs and act upon KPIs to enhance performance. 8. Ensure best practices are shared across Novartis CPO medical organizations and the global team. Provide information related to C4 insights for medical affairs team and other departments 9. Compile and select published evidence for products to support answers to Health Authorities, such as license renewals (e.g., for Clinical Expert Statements) or Periodic Safety Update Reports in cooperation with the responsible departments 10. Responsible for overall talent and career development of talent within the team by designing and implementing training plans.Minimum requirementsMinimum: Bachelor degree in a healthcare related field with medical information or communication skills. Will consider other scientific degree plus strong medical information and communication skill English: fluent oral and written +5 years of experience in medical communication / writing settings Strong medical writing skills with history of creating clear, concise, and compelling medical letters Skills in defining specific search strategies in commonly used databases such as PubMed, Ovid, STN, etc.( including adequate use of Boolean operators, nested searches, field operators/descriptors, database-specific medical thesaurus in order not to miss important data while at the same time limit hits to specific data on any specific medical or scientific topic.) Profound understanding of scientific and medical language and quality standards used in published literature (allowing understanding and selecting adequate data in a particular context of question and to judge on reliability or level of evidence of such data). Ability to drive functional excellence within the team Strong customer focus General knowledge of therapy area and products Strong cross-functional perspective.,
Keyskills :
core datawriting skills adverse eventsmedical writing medical affairsquality standards information systemcareer development