Impress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.
Tailor your resume to this Clinical Research Spec role.
Rezi rewrites your resume against Medtronic's job description. Free.

Tailor your resume to this Clinical Research Spec role.
Rezi rewrites your resume against Medtronic's job description. Free.
Don't guess if your resume is good enough.
See how it scores against the Clinical Research Spec posting at Medtronic — free, in seconds.

Don't guess if your resume is good enough.
See how it scores against the Clinical Research Spec posting at Medtronic — free, in seconds.
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 documents.
- Build strong relationships with internal and external stakeholders.
- Report and respond to serious adverse events, deviations, and medical device malfunctions.
- Perform other duties as required by the organization or project.
Requirements
- Minimum of 5 years of clinical trial monitoring experience in a medical device company, pharmaceutical company, or CRO.
- Experience managing key accounts at major hospitals.
- Deep knowledge of GCP.
- Ability to read SOPs and 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.
- Willingness to continuously learn.
- Ability to travel for overnight business trips and handle unexpected external work.
- Availability to attend global meetings early in the morning or late at night.
- Ability to respond quickly to urgent situations such as serious adverse events.
Skills
- GCP knowledge
- English reading and writing
- Communication skills
- Problem-solving skills
- Proactive and autonomous work style
- Teamwork
- Continuous learning
- ISO 14155 knowledge
Location
- Tokyo or Osaka
- Nationwide (for assigned facilities)
Work Type
- Hybrid (minimum 1 day/month in office)
- Full-time
Experience Level
- 5+ years of clinical trial monitoring experience
- Experience as a team leader
- Experience training new or junior monitors
- Experience in KOL management within the disease area of assigned trials
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
- Childcare cost support up to ¥360,000 per year
- 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
- Annual paid leave
- Industrial accident leave
- Menstrual leave
- Maternity leave
About the Company
- Global leader in healthcare technology.
- Mission to alleviate pain, restore health, and extend life.
- Operations in over 150 countries.
- 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.