Clinical Study (project) Manager (crms @ Tokyo)

Medtronic UK

Tokyo, Japan
J-gcp/iso14155
Clinical trial acts
Managing external suppliers
You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world

Job Summary

  • You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
  • The Clinical Research Medical Science Department (CRMS) is responsible for the evaluation/assessment of the safety and efficacy of new medical devices through domestic and global clinical research/trial.
  • Medtronic offers comprehensive benefits and compensation programs designed to enhance the financial, physical, and mental well-being of each employee.

Matching Summary

You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

Skills & Requirements

Must-have

  • J-GCP/ISO14155
  • Clinical trial Acts
  • managing external suppliers
  • Project Management
  • English business level
  • Japanese native level

Nice-to-have

  • medical field experience
  • medical knowledge
  • PMDA GCP inspection experience
  • CRA experience
  • device and disease knowledge
  • statistical analysis
  • data management
  • embrace diversity
  • multi-cultural stakeholders

Key Requirements

  • 5+ years J-GCP/ISO14155, Ethical Guidelines, Clinical trial Acts
  • 3+ years managing external suppliers
  • Project Management experience
  • Bachelor’s Degree

Work Rights

Not specified

Tailored Resume

Cover Letter