Work Location , Expected Annual Income :
Tokyo,8.0M ～ 10.0M
About the Company :
Global European Clinical Research Service Start-up
Responsibilities :
Responsibilities:
-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
Benefits :
Employment Type: Full Time Employee
Office Location: Tokyo
Working Style: Hybrid
Budget: up to 10mil.
Interview Steps: 3
Working Language: English and Japanese
Welfare and Insurance: Covered
Required Experience / Abilities / Skills :
Requirements:
-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)