- Provide support for medical safety management within the IMS Department, including single case medical review and related activities, aggregate reports including coordination and management of large datasets for analysis purposes, and preparation of responses to Health Authorities, within agreed timeframes and to a high standard of accuracy, in compliance with DS&E business rules, standard operating procedures and global and local regulatory requirements. Performs signal detection for assigned products in the Empirica Signal tool. Provide input to medical safety aspect for dedicated projects, lead internal management teams such as SPT or SMT1. Performs medical review of single cases from all sources, including review of events associated to quality defects 2. Manages or supports the preparation and review of Investigator Notifications 3. Performs signal detection and signal evaluation activities for assigned products 4. Co-authors and contributes to the medical sections of periodic reports (PBRER, DSURs per project assignment), assists in or leads the preparation of other safety related documents, including Investigator Brochures (IB), Core Data Sheets (CDS), Product Guidance Documents (PGD), Expert Statements, and Responses to Health Authorities inquiries 5. With BSL/ PVLs support, assist in the development, maintenance and implementation of RMP including the coordination with other line functions for associated activities such as updates, management of large datasets for analysis purposes and the ongoing tracking of commitments and effectiveness measures. The PVE will assume increasingly independent ownership of these processes 6. Regularly assists to interface with the clinical team for safety matters, including follow-up on events of interest, input into site queries regarding adverse events, and updating Team on PVO requirements 7. Supports the BSL/ PVL/ Sr. PVE as per project assignment, as an IMS contact at internal management teams as SPT, SMT, and GPT 8. Supports preparation for and participates on internal safety reviews boards, such as SMT, MSRB, and SIGDET 9. Provides support to BSL/ PVL/ Sr. PVE for quality assurance activities, internal audits, and Health Authority inspections10. Quality of work delivered (attention to details, thoroughness, medical sound judgment, and medical writing skills)11. Writing concise, accurate and quality documents 12. Timeliness of deliverables according to established directives 13. Compliance with Internal and external regulations and procedures 14. High level of independence 15. Effective communication with- and support to- product safety Colleagues and project functions
Company Profile:
Novartis Healthcare Pvt. Ltd.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding
in our field.