Clinical Research Monitor
Medtronic · Limburg, Netherlands
The apply link worked recently (not employer-confirmed).
Role summary
A Clinical Research Monitor ensures medical device clinical trials are conducted in compliance with protocols, regulatory requirements, and company procedures at investigational sites. The role involves monitoring trial progress, managing relationships with investigators and research institutions, reviewing adverse events, and supporting study documentation. This position requires a bachelor's degree in Clinical Research, Engineering, or Life Sciences plus at least two years of relevant industry experience, fluency in English and Dutch, and strong project management capabilities.
What they're looking for
- Bachelor's degree in Clinical Research, Engineering, or Life Sciences
- At least 2 years of clinical research monitor experience in medical device industry
- Fluent in English and Dutch languages
- Strong interpersonal skills and ability to manage multiple concurrent projects
- Proficiency with IT tools, applications, and Microsoft Office
- Knowledge of applicable regulations, healthcare industry, and medical terminology
What you'll be doing
- Monitor clinical trial progress at site or headquarters level for protocol and regulatory compliance
- Develop and maintain relationships with investigators, CROs, hospitals, and research institutions
- Review adverse event cases and monitor study timelines, budgets, and schedules
- Prepare study documentation and issue status reports as needed
- Train investigators and site personnel on clinical research procedures and requirements
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.