Job description
Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role: This role can be based in our White City, London office (hybrid working, 3 days per week) or the Novartis Schaftenau site in Austria. As Global Program Regulatory Manager Precision Medicines you will be responsible for the successful implementation of strategic IVD regulatory plans and innovative regulatory solutions. You will achieve timely submissions/approvals and to adhere to regulatory requirements. The GPRM Precision Medicines works with some independence to provide regulatory support including tactical and technical regulatory direction for projects within the Precision Medicine (PM) business of Novartis Development and Biomedical Research programs as they relate to IVDs; including tactical support to the PM associates to ensure execution of the Dx regulatory plans in line with the therapeutic global strategy and in collaboration with the RA lead on the Global Program Team. The GPRM coordinates, reviews, and may prepare reports for submission.
Address
Form of work
London, England
