Senior Scientific Information Manager II
Novartis - Hyderabad, Andhra Pradesh
1. Develop and 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-GSI 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.
For more info visit at mentioned link
Novartis - Hyderabad, Andhra Pradesh
1. Develop and 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-GSI 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.
For more info visit at mentioned link
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