Job Description

A Study Manager in the life science industry will oversee clinical study operations, ensuring projects are executed efficiently and meet compliance standards. This role in Tokyo requires a strong understanding of healthcare regulations and the ability to manage cross-functional teams effectively.

職務内容

* Plan, coordinate, and manage clinical studies to ensure timely completion within budget and scope.
* Oversee study protocols and ensure adherence to regulatory guidelines and ethical standards.
* Collaborate with cross-functional teams, including medical, regulatory, and operational departments.
* Manage vendor relationships and ensure the quality of outsourced services.
* Monitor study progress, including risk assessment and mitigation strategies.
* Prepare and present study updates and reports to stakeholders.
* Ensure proper documentation and data integrity throughout the study lifecycle.
* Support the development and implementation of innovative study practices and tools.

理想の人材

A successful Study Manager should have:

* A degree in life sciences, healthcare, or a related field.
* Proven experience in clinical study management within the life science industry.
* Familiarity with healthcare regulations and compliance requirements.

条件・待遇

* Competitive annual salary ranging from JPY 8100000 to JPY 9900000.
* Hybrid work environment offering flexibility.
* Opportunities to work on impactful healthcare projects in Tokyo.
* Supportive company culture focused on innovation and excellence in life science.
* Comprehensive benefits package tailored to employee well-being.

Page Group Japan is acting as an Employment Agency in relation to this vacancy. A degree in life sciences, healthcare, or a related field.
Proven experience in clinical study management within the life science industry.
Familiarity with healthcare regulations and compliance requirements.

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