Job description
Our Regulatory Operations Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are simplifying 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 in evolving the future of Regulatory Operations and to give our patients and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role: This role offers hybrid working, requiring 3 days per week in person in our White City, London office. Ad-hoc working hours to overlap the US as required. As a Global Regulatory Publishing Associate, you will be accountable for all clinical document/report and submission dossier publishing, verification, dispatch, and coordination of HA compliant, worldwide HA submissions in support of Novartis global product portfolios.
Address
Form of work
London, England
