Job Description SummaryContribute to the overall activities in drug development* toward obtaining the marketing authorization and maintenance activities of post marketing products in assigned TA area. * Drug development including development of drug, medical device, companion
Job Description SummaryAs a CMC development specialist, enhance Japan’s CMC development strategy by offering scientific and technical support to global/local CMC development teams and other departments, while keeping up with the latest technological advancements. [Note] 1:
Job Description SummaryAccountable for the oversight and coordination of program and study level (re-)feasibility assessments in the country, in collaboration with program and/or trial feasibility teams, in compliance with Novartis processes, GCP, ICH and regulatory requirements.
Job Description Summary To manage business and operational activities of local regulatory writing (RW) to ensure timely production of high quality clinical documentation. To ensure compliance with global RW strategy and implementation of technical activities &
