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| Hiring Company | PSI CRO Japan株式会社 | 
| Location | Tokyo - 23 Wards | 
| Job Type | Permanent Full-time | 
| Salary | 5 million yen ~ 8 million yen | 
【求人No NJB2302347】
Take your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time. 
You will: 
Maintains study specific and corporate startup tracking systems
Facilitates site budgets and contract negotiations
Supports site regulatory document collection
Under supervision  may prepare initial submission dossiers to competent authorities  ethics committees  and/or site submission dossiers (as applicable)
Communicates with the project team and investigational sites throughout the study startup phase
Develops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestones
May review study specific translations
Supervises Trial Master File (TMF) maintenance throughout the study startup phase
| Minimum Experience Level | No experience | 
| Career Level | Mid Career | 
| Minimum English Level | Business Level | 
| Minimum Japanese Level | Native | 
| Minimum Education Level | Bachelor's Degree | 
| Visa Status | Permission to work in Japan required | 
College/University degree in Life Sciences or an equivalent combination of education  training and experience
2 3 years prior clinical study and site startup experience
Well developed communication and organizational skills
Ability to negotiate and build relationships at all levels
Leadership  mentoring  and organizational skills
English and Japanese skills (High Business level to Fluent)
| Job Type | Permanent Full-time | 
| Salary | 5 million yen ~ 8 million yen | 
| Work Hours | 09:00 ~ 18:00 | 
| Holidays | 【有給休暇】初年度 最大10日(入社月によって異なる) 【休日】完全週休二日制 土 日 祝日 年末年始 | 
| Industry | Contract Research Organization | 
| Company Type | International Company |