Listed on Medtronic’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role supports clinical trials for a global medical device company, managing trial sites, monitoring compliance, and ensuring regulatory adherence across Japan. It suits someone with 5+ years of trial monitoring experience who can coordinate between research sites and internal teams while handling documentation, audits, and adverse event reporting.
Our summary, not Medtronic’s wording. The full posting is on their site.
What they ask for
Required
- 5+ years of clinical trial monitoring experience at a medical device company, pharmaceutical company, or CRO
- Experience managing major hospital sites
- Deep knowledge of GCP
- Ability to read SOPs and business documents in English and write monitoring reports
- High compliance and quality awareness
- Strong communication and problem-solving skills
- Self-directed and proactive approach
- Teamwork orientation
- Commitment to continuous learning
- Bachelor's degree or higher
Nice to have
- Experience in cardiovascular or vascular disease areas
- Team leadership experience
- Experience training junior monitors
- KOL management experience in trial disease area
- Knowledge of ISO 14155