Sr Clinical Research Spec
Medtronic · Tokyo, Japan
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
What they're looking for
- Seven-plus years of clinical trial monitoring experience at medical device, pharmaceutical, or CRO companies
- Experience leading monitoring teams of three or more staff members
- Track record managing core teaching hospitals and major medical institutions
- Deep knowledge of GCP guidelines and regulatory requirements
- English proficiency for SOP reading and monitoring report writing
- Bachelor's degree or higher in medicine, pharmacy, nursing, life sciences, or engineering
- Strong compliance awareness and quality assurance mindset
What you'll be doing
- Plan, execute, and manage clinical trials, post-market research, and post-market surveillance with progress reporting
- Conduct on-site procedures, monitoring activities, and audit responses at assigned facilities
- Lead monitoring teams and mentor junior or less-experienced monitors through coaching
- Report and respond to serious adverse events, protocol deviations, and device defect notifications
- Create and review regulatory documentation 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.