Clinical Study (project) Manager (crms @ Tokyo)

Medtronic

Tokyo, Japan
On-site
J-gcp/iso14155 compliance
External supplier management
Project management experience
Medtronic is seeking a Clinical Study Manager in Tokyo to lead clinical teams in executing various clinical studies, ensuring compliance with regulatory requirements. The ideal candidate will have extensive experience in clinical research and project management within the medical field, and they will benefit from a comprehensive benefits package

Job Summary

  • Lead clinical teams to execute various clinical studies, develop strategies, and collaborate with internal and external stakeholders.
  • Manage ongoing and new clinical research/trials, including supplier selection, milestone management, data collection, and budget planning.
  • Medtronic offers comprehensive benefits and compensation programs designed to enhance employee well-being, including childcare subsidies and career development opportunities.

Matching Summary

Match Score: 85

Medtronic is seeking a Clinical Study Manager in Tokyo to lead clinical teams in executing various clinical studies, ensuring compliance with regulatory requirements. The ideal candidate will have extensive experience in clinical research and project management within the medical field, and they will benefit from a comprehensive benefits package.

Skills & Requirements

Must-have

  • J-GCP/ISO14155 compliance
  • external supplier management
  • project management experience
  • strong communication skills
  • problem-solving and analytical skills
  • business level English

Nice-to-have

  • medical field experience
  • medical knowledge
  • PMDA GCP conformity inspection experience
  • CRA experience
  • device and disease knowledge
  • statistical analysis knowledge
  • data management knowledge

Key Requirements

  • 5+ years of experience in J-GCP/ISO14155
  • 3+ years of experience managing external suppliers
  • Bachelor's Degree

Work Rights

Not specified

Tailored Resume

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