Clinical Research Spec
Medtronic · Tokyo, Japan
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Medtronic seeks a Clinical Research Specialist in Tokyo to manage clinical trials and post-market studies across Japanese healthcare facilities. The role involves monitoring trial operations, ensuring regulatory compliance, managing site relationships, and coordinating safety reporting.
What they're looking for
- 5+ years clinical trial monitoring experience at medical device, pharmaceutical, or CRO organizations
- Experience managing flagship hospitals or major medical centers
- Deep knowledge of GCP guidelines and regulatory requirements
- English proficiency for reading SOPs and writing monitoring reports
- Bachelor's degree in medicine, pharmacy, nursing, life sciences, or engineering
- Strong communication, problem-solving, and compliance awareness
- Self-directed, proactive, and collaborative working approach
What you'll be doing
- Plan, implement, and manage clinical trials, post-market studies, and reporting documentation
- Conduct site monitoring, audit coordination, and facility procedures at trial locations
- Create and verify regulatory and procedural documents
- Report and respond to serious adverse events, protocol deviations, and device malfunctions
- Build and maintain relationships with internal and external stakeholders
Privacy & handoff
This role links to Medtronic's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.