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| Hiring Company | 再生医療ベンチャー | 
| Location | Tokyo - Other Areas | 
| Job Type | Permanent Full-time | 
| Salary | 12 million yen ~ Negotiable, based on experience | 
【求人No NJB2136353】
This position reports directly to the Vice President who is responsible to manage all resources and budgets for global activities initiation  and reports dotted to President and works together to present/discuss regulatory strategy with key stakeholders. This position will lead designing regulator strategy global together with Business Unit Head  BU Head  who is responsible to lead an asset team. This position will be a liaison with oversea’ regulatory authorities for obtaining regulatory’ buy in and support clinical trial execution outside of Japan. This position is individual contributor in principle  however  will work closely with the local regulatory specialist who works as local liaison for PMDA in Japan and reports to in charged BU Head.
| Minimum Experience Level | No experience | 
| Career Level | Mid Career | 
| Minimum English Level | Native | 
| Minimum Japanese Level | Native | 
| Minimum Education Level | Bachelor's Degree | 
| Visa Status | Permission to work in Japan required | 
Qualifications
1. BA/BS degree required
2. Minimum 10+years of overall business experience
3. Minimum 5+years of R D regulatory experience including lead liaison
assignment for outside Japan regulatory filing and IND management  such as
in US.
4. Preferable experience to discuss any priority/acceleration discussion with
regulatory authorities
5. Must be able to partner effectively and influence at all levels in a matrix
environment with strong interpersonal skills and effectiveness.
| Job Type | Permanent Full-time | 
| Salary | 12 million yen ~ Negotiable, based on experience | 
| Holidays | 【有給休暇】初年度 10日 1か月目から <休日> 日曜日、土曜日、国民の祝日に関する法律に定められた休日、会社が指定する日 … | 
| Industry | Pharmaceutical |