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About the Role
Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
Responsibilities
- Manage and report on clinical trials, post-market clinical research, and post-market surveillance.
- Handle procedural tasks, monitoring, and audit responses at assigned facilities.
- Create and review relevant documentation.
- Build strong relationships with internal and external stakeholders.
- Report and manage serious adverse events, deviations, and medical device malfunctions.
- Perform other duties as required by the organization or project.
Requirements
- Over 5 years of clinical trial monitoring experience in medical device, pharmaceutical, or CRO companies.
- Experience managing accounts at core hospitals such as university hospitals.
- Deep knowledge of GCP.
- Ability to read SOPs and work-related documents in English and create monitoring reports in English.
- High compliance and quality awareness.
- Excellent communication and problem-solving skills.
- Ability to think proactively and act autonomously.
- Ability to prioritize teamwork and collaborate effectively.
- Proactive learning attitude.
Skills
- Clinical trial monitoring
- GCP knowledge
- English proficiency (reading, writing reports)
- Communication skills
- Problem-solving skills
- Proactive thinking
- Teamwork
- Continuous learning
- ISO 14155 knowledge
Location
- Tokyo
- Osaka
- Nationwide (for assigned facilities)
Work Type
- Hybrid (minimum 1 day/month in office)
- Business travel required (including overnight stays)
- Flexibility for early/late global calls
- Ability to respond quickly to urgent situations (e.g., serious adverse events)
Experience Level
- 5+ years of clinical trial monitoring experience
- Experience in cardiovascular or cardiothoracic fields (preferred)
- Team leader experience (preferred)
- Experience training new or junior monitors (preferred)
- KOL management experience in the disease area of the trial (preferred)
Education Level
- Bachelor's degree or higher in medicine, pharmacy, nursing, life sciences, or engineering fields.
Salary/Compensations
- Competitive Salary
- Eligible for Medtronic Incentive Plan (MIP)
Benefits
- Annual childcare support up to ¥360,000
- 6 weeks of leave for family caregiving or adoption
- Babysitter and daycare matching services
- Career development including mentoring programs and e-learning
- Internal career network supporting women's advancement
- Employee stock purchase plan
- Commuting allowance
- Overtime allowance
- Holiday work allowance
- Competitive Benefits Package
About the Company
- Global leader in healthcare technology.
- Mission to alleviate pain, restore health, and extend life.
- Operations in over 150 countries with 95,000 employees.
- Develops innovative medical technologies improving the lives of over 72 million patients annually.
Equal Opportunity
- Medtronic offers a competitive Salary and flexible Benefits Package.
- A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.