非公開
1. Lead to design global regulatory strategy for both development assets; cardiomyocyte and pancreatic islet cell.
2. Support BU Head to design filing data package globally.
3. Be responsible liaison when company talks with regulatory authorities outside of Japan such as FDA for any topics including an appropriateness of CMC data package and pre-clinical data package for IND opening, study design for support regulatory claim
4. Work together with President directly, present and discuss any regulation related matter including possibility of acceleration with global key stakeholders such as investors/shareholders/key opinion leaders/media, or so on.
5. May lead/join any corporate-wide task to meet company’ vision-mission-purpose.
高いiPS細胞技術を持つ成長中企業です。