薬事臨床開発部／クリニカル＆メディカルアフェアーズ担当（cama/tokyo）

ZEISS Group

Tokyo, Japan
Base: 350,000 - 520,000 jpy monthly; bonus/equity:...
Clinical trial experience in medical devices
Ophthalmology knowledge or clinical practice
Creation of clinical trial documents
The role involves managing the full lifecycle of clinical trials including document creation, site monitoring, and CRO management

Job Summary

  • The role involves managing the full lifecycle of clinical trials including document creation, site monitoring, and CRO management.
  • Candidates must possess specific expertise in ophthalmology or have experience creating regulatory submission documents like STED.
  • The position offers a competitive salary range of 5 to 7.5 million yen annually along with comprehensive benefits including health insurance and discounts on optical products.

Matching Summary

The role involves managing the full lifecycle of clinical trials including document creation, site monitoring, and CRO management.

Salary

Base: 350,000 - 520,000 JPY monthly; Bonus/Equity: Annual bonus included; Benefits: Cafeteria points, travel allowance up to 50,000 JPY, health insurance, optical discounts

Skills & Requirements

Must-have

  • Clinical trial experience in medical devices
  • Ophthalmology knowledge or clinical practice
  • Creation of clinical trial documents
  • Regulatory submission document creation
  • English communication skills

Nice-to-have

  • GCP compliant monitoring skills
  • Knowledge of clinical research laws
  • Intermediate to business level English
  • Experience with strategic planning

Key Requirements

  • Medical device clinical trial experience
  • Ophthalmology knowledge or vision training certification
  • Ability to read English literature and communicate via email

Work Rights

Not specified

Tailored Resume

Cover Letter