Clinical Study Manager

Publication date 2026/02/16

Work Location , Expected Annual Income :

Tokyo,Osaka,10.0M ～ 12.0M

About the Company :

Global European Pharmaceutical Manufacturer

Responsibilities :

Job Description
Responsible for leading and managing clinical delivery team of contributing experts to operationally deliver defined clinical studies, or clinical project work package / activities to time, cost and appropriate quality in Japan R&D.

Clinical Operations is the organisational home for the operational delivery and programme and project management of clinical projects, drug and non-drug.

Skill-set
- Excellent Communication and relationship building skills
- Proven ability to prioritize and manage multiple tasks with conflicting deadlines
- Excellent interpersonal skills and proven ability to facilitate team building and team work
- Proactively identifies risks and issues and possible solutions
- Demonstrates ability to prepare and deliver study related training materials
- Demonstrates ability to plan, coordinate, and facilitate internal and external meetings
- Demonstrates professionalism and mutual respect
- Displays excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high volume environment with shifting priorities
- Proven learning agility
- Basic knowledge and experience of quality management

Nice to have
- Project management certification
- Ability to interact widely and effectively within the company at all levels. Good networking skills
- In-depth knowledge of clinical and drug development process
- Fiscal and financial awareness

Benefits :

Employment Type: Full time Employee
Office Location: Tokyo or Osaka
Working Style: Hybrid
Budget Range: Up to 12mil
Interview Steps: 3
Welfare and Insurances: Covered.

Required Experience / Abilities / Skills :

Experience
Mandatory
- At least 5 years’ experience from within the pharmaceutical industry or similar organization or academic experience.
- Extensive knowledge of clinical operations, project management tools and processes
- Understanding of the skills and knowledge required for the successful delivery of a clinical study, e.g. ICH-GCP/J-GCP, local regulations, study management
- Good experience of clinical development / drug development process in various phases of development and therapy areas


Nice to have
- Working experiences in Clinical Development/ Quality Assurance, especially Oncology experience
- Knowledge of process improvement methodology such as Lean Sigma/Change Management


Education
- Bachelor’s Degree in Science or related discipline

Nice to have
- Medical or biological sciences or discipline associated with clinical research.
- Advanced degree is preferred.

Contact Information :

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

If you are interested, please email us for an inquiry!

JOB ID : IJB2011349