早期臨床開発の安全性を担当するメディカルドクター / Medical Doctor responsible for safety in early clinical development

Background of recruitment：

To strengthen the safety function in early clinical development.

Description of work：

Responsible for safety management in early clinical development of our proprietary products, contributing to global pharmaceutical development. 応募資格／Qualifications 求める経験：

5年の臨床従事期間（必須）

TOEIC L&Rスコア800点以上相当の英語力（日本語を母国語とする場合）

Required Qualification：

At least 5 years of clinical practice experience as a physician (mandatory).

Experience in in vitro / in vivo studies (mandatory).

Experience as a postdoctoral research fellow.

Preferred Knowledge and Skills：

Logical thinking ability

Advanced negotiation skills with internal and external stakeholders

Curiosity and flexibility

Who You Are：

Be willing to have proactive communication and initiative, and take on challenging goals as a team member

Be willing to have a global perspective and contribute to organizational and human resource development based on your knowledge and experience as a medical professional

Be willing to have a humble and curious attitude to proactively learn about areas outside the medical field

Desired Qualification：

Medical license (foreign medical license is also acceptable).

Board certification in a specific disease area.

Doctor of Medicine (Ph.D.) (Experience in basic research).

Publication of original research papers in English as the first author.

English proficiency equivalent to TOEIC L&R score of 800 or above (for native Japanese speakers).

Position Features：

Opportunity to contribute to global healthcare through drug safety management.

Opportunity to utilize both medical / scientific background and English proficiency. 待遇／Salary & Benefits 当社規定により優遇いたします

To be decided in accordance with our criteria

Flextime system

The notification of working conditions will be made in an electronic file.

If you apply, please understand this point.