Clinical Study Startup Specialist

Publication date 2026/03/3

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)

Contact Information :

JAC International, Healthcare Team
Mark Miller
Email: m-miller@jac-international.jp

If you are interested, email us for an inquiry!

JOB ID : IJB2008839