# Clinical Research Spec

Hiring organization: [Medtronic](https://career.thegoodapps.co/organizations/medtronic)

Canonical page: https://career.thegoodapps.co/jobs/ace35936-54d3-4899-90b3-63b9ab9e8a12

Listed on Medtronic's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Mid

## Summary

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._

## 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

Apply on Medtronic's site: https://medtronic.wd1.myworkdayjobs.com/en-US/MedtronicCareers/job/Tokyo-Tokyo-Japan/Clinical-Research-Specialist--CRMS---Tokyo-_R58711-1