Job Description

The Sr Clinical Development Lead will oversee the strategic planning and execution of clinical development programs in the life sciences industry. This position is based in Tokyo and requires a strong understanding of clinical research and regulatory processes.

職務内容

* Lead the design and implementation of clinical development plans for assigned programs.
* Collaborate with cross-functional teams to ensure alignment on program objectives and timelines.
* Oversee clinical trial activities, including protocol development and site management.
* Ensure compliance with regulatory requirements and ethical standards in clinical research.
* Analyze clinical data and provide strategic recommendations to stakeholders.
* Manage relationships with external partners, such as CROs and investigators.
* Contribute to the preparation of regulatory submissions and presentations.
* Support the development of team members through mentorship and guidance.

理想の人材

A successful Sr Clinical Development Lead should have:

* A degree in life sciences, medicine, or a related field.
* Extensive knowledge of clinical development processes and regulatory guidelines.
* Proven experience in managing clinical trials and cross-functional teams.
* Strong analytical and problem-solving skills.
* Excellent communication and interpersonal abilities.
* Fluency in English; proficiency in Japanese is an advantage.
* Experience in the life sciences industry is highly desirable.

条件・待遇

* Hybrid working model for flexibility and work-life balance.
* Comprehensive benefits package, including health insurance and retirement plans.
* Opportunities for professional development and career growth.
* Engaging and collaborative work culture in Tokyo.

This role offers an exciting opportunity to contribute to groundbreaking advancements in the life sciences industry. Interested candidates are encouraged to apply and be part of a team that makes a difference.

Page Group Japan is acting as an Employment Agency in relation to this vacancy. A degree in life sciences, medicine, or a related field.
Extensive knowledge of clinical development processes and regulatory guidelines.
Proven experience in managing clinical trials and cross-functional teams.

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