Clinical Research Monitor
Medtronic
•Remote
About The Position
Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. As a Clinical Research Associate, you will be responsible for monitoring clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory requirements, the policies of the ethics committee, and Medtronic procedures. You will work closely with Medtronic study management teams as well as site staff to resolve issues and ensure the smooth conduct of clinical studies. You would ideally be based in the Netherlands.
Requirements
- Bachelor degree in Clinical Research, Engineering, or Life Sciences
- At least 2 years of experience as a Clinical researcher monitor in the Medical device industry
- Fluent in English and Dutch
- Strong interpersonal skills and comfortable working in a team
- Ability to identify priorities and manage deadlines across multiple projects simultaneously
- Proficiency with IT tools, applications, and Microsoft Office
- One to four years of experience in clinical research
- Knowledge of applicable regulations and standards
- Knowledge of the healthcare industry
- Knowledge of medical terminology
- Problem-solving skills
Responsibilities
- Monitors the progress of clinical trials at site or headquarters level, ensuring they are conducted, documented, and reported according to the protocol, SOPs, GCP, and applicable regulatory requirements
- Develops and maintains relationships with clinical investigators, CROs, affiliated hospitals, and research institutions to support the initiation and advancement of clinical studies
- Reviews adverse event cases with investigators and monitors study timelines, budgets, and schedules
- Prepares study documentation and issues status reports as needed
- Assists with the design, development, and monitoring of clinical evaluation projects
- Trains investigators and site personnel, including both headquarters and field clinical research associates
- Supports the clinical development strategy, identifies and recommends qualified investigators, initiates clinical trials, and helps ensure patient recruitment and retention
Benefits
- Competitive Salary
- Flexible Benefits Package
- Medtronic Incentive Plan (MIP)
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
