**Basic purpose of the job**


To contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization.

**Accountabilities**


・Strengthen the profile of our products by providing medical/scientific robust guidance in the responsible therapeutic area through the total process of the clinical development phases, in collaboration with Global and other departments.


・Ensure and support Japanese submission and registrations in the respective products collaborating with regulatory/ clinical development team. (Support the clinical part until approval, such as preparation of responses to PMDA queries.)


・Responsible for making Japanese clinical development plan recognized by global Medicine as well aligned with global development strategy in the respective therapeutic area.


・Suppor...