Associate safety operations adviser

Department :Global Safety. Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can:do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment. About the Department Global Safety, Bangalore has global responsibility for surveillance of Safety and Quality of Novo Nordisk clinical development and marketed Products and is responsible for global handling and reporting of adverse events reports. The Position All tasks in the GS:GBS SO Safety Operations Advisers department demand a large professional insight, self:dependence, and competence in making decisions, as well as flexibility, a good comprehensive view and a many:functioned, often international, co:operation. Ensure the fulfilment of global regulatory requirements to the collection, evaluation and reporting of safety information on Novo Nordisk (NN) pharmaceutical products i.e., spontaneously reported adverse events, serious adverse events (SAEs) from clinical trials, investigator sponsored trials, named patient supplies and third:party trials, ensure appropriate medical interpretation and evaluation of adverse events reported from world:wide sources, from marketed use. To contribute to the collection, medical evaluation, and reporting (to the authorities) concerning adverse events from clinical use of Novo Nordisk s preparations and products in the post approval phase. The tasks demand a large professional insight, self:dependence and competence in making decisions, as well as flexibility, a good comprehensive view and a many:functioned, often international, co:operation.To be responsible for immediate reporting to the relevant authorities of serious adverse events that may be associated with Novo Nordisk s products. Omission or a delay to do so can result in serious consequences for Novo Nordisk.To be responsible for the medical evaluation of reports concerning serious adverse events, as well as for the evaluation of possible causal relationships. : To ensure the review and preparation of relevant follow up questions, consistency in handling clinical and post:marketing cases. To escalate critical adverse events/reactions to line manager and/or Safety Surveillance Adviser. Medical evaluation and medical review on all case types, as applicable. To review AE, pregnancy, and safety information forms (both electronic forms and paper forms). Monthly review of spontaneous non :serious cases as non:cases as non:serious line listings to ensure consistency in coding and listedness. : To participate in clinical project groups as well as safety meetings as needed and to ensure responsible coverage of safety areas. To review clinical protocols to ensure that all relevant safety information is captured through the procedures described in the protocol and to ensure that these procedures are in alignment with the workflow in Safety Operations. Point of contact providing support for Data Management colleagues if/when product queries arise. : To ensure accurate and consistent coding using MedDRA of all adverse events reported NN to ensure consistency and precision between projects, products and countries in the coding of adverse events. To ensure the review and preparation of relevant follow up questions. : To participate in the GS MedDRA Coding Group and Case Handling meetings as required. To ensure up:to:date knowledge through participation in relevant courses and meetings and through reading relevant literature, regulatory guidelines and new media. To supervise reconciliation process of SAEs with the clinical trial data base. Ensure all tasks are performed in compliance to and in accordance with Good Clinical Practic