Principal Responsibilities ・Accountable as Regulatory Lead to develop and implement regulatory strategies for assigned product(s)/project(s) in Japan and accountable to provide regulatory advice to cross-functional strategies and associated deliverables according to business objectives. ・Lead the planning
ジェンマブは、革新的で独自性のある抗体治療薬の開発に注力し、患者さんの人生をより豊かにすることを目的としています。 The Nonclinical Safety & Toxicology Team are looking for an experienced toxicologist fluent in both English and Japanese who will be based in Japan for a newly created position as sponsor monitor for nonclinical safety
1. Basic Purpose of the Position In order to develop veterinary biological products, conduct necessary studies and compile submission dossiers, including CMC part, (under the supervision of superiors, in case of Associate Scientist). In addition, expanding the
Principal Responsibilities Accountable as Regulatory Lead to develop and implement regulatory strategies for assigned product(s)/project(s) in Japan and accountable to provide regulatory advice to cross-functional strategies and associated deliverables according to business objectives. Lead
