Clinical Research Spec

Medtronic UK

Tokyo, Japan
5+ years clinical trial monitor experience
Gcp knowledge
English sop reading and report writing
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 Monitoring Department plays a crucial role in supporting the advancement of clinical research in collaboration with the CRMS department.
  • Medtronic offers a competitive Salary and flexible Benefits Package, including annual childcare support and career development programs.

Matching Summary

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

Skills & Requirements

Must-have

  • 5+ years clinical trial monitor experience
  • GCP knowledge
  • English SOP reading and report writing
  • High compliance and quality awareness
  • Excellent communication and problem-solving skills
  • Proactive and self-motivated
  • Teamwork and collaboration

Nice-to-have

  • Cardiovascular or cardiac experience
  • KOL management experience
  • PMDA face-to-face consultation experience
  • PMDA regulatory affairs experience
  • ISO 14155 knowledge

Key Requirements

  • 5+ years clinical trial monitor experience in medical device, pharmaceutical, or CRO
  • Experience with university hospitals or major medical institutions
  • Bachelor's degree (Medicine, Pharmacy, Nursing, Life Science, Engineering preferred)
  • English proficiency for document reading and report writing
  • Hybrid work model (minimum 1 day/month in office)

Work Rights

Not specified

Tailored Resume

Cover Letter