Clinical Research Monitor: Elevate Trials (NL)

Medtronic; Maastricht; On-site; EUR 42,000 - 65,000; Full time

Job summary

Medtronic Maastricht is seeking a Clinical Research Associate to monitor investigations at sites, ensuring adherence to protocols, regulatory requirements, and Medtronic procedures. You will work closely with study management teams and site staff to resolve issues and ensure smooth conduct of clinical studies.

You will collaborate with investigators, CROs, and research institutions to support initiation and advancement of clinical studies, review adverse events, and monitor timelines and

Qualifications

• Bachelor degree in Clinical Research, Engineering, or Life Sciences with at least 2 years as a clinical researcher monitor.
• Fluent in English and Dutch.
• Strong interpersonal skills and ability to work in a team and manage deadlines across multiple projects.
• Proficiency with IT tools, applications, and Microsoft Office.
• 1–4 years of experience in clinical research with knowledge of applicable regulations and healthcare terminology.

Responsibilities

• Monitor the progress of clinical trials at site or HQ level, ensuring they are conducted, documented, and reported according to the protocol, SOPs, GCP, and applicable regulatory requirements.
• Develop and maintain relationships with clinical investigators, CROs, affiliated hospitals, and research institutions to support initiation and advancement of clinical studies.
• Review adverse event cases with investigators and monitor study timelines, budgets, and schedules.
• Prepare study documentation and issue status reports as needed.
• Train investigators and site personnel, including both headquarters and field clinical research associates.
• Support the clinical development strategy, identify and recommend qualified investigators, initiate clinical trials, and help ensure patient recruitment and retention.

Skills

Fluent English

Fluent Dutch

Interpersonal skills

MS Office

Education

Bachelor degree in Clinical Research, Engineering, or Life Sciences

Tools

Microsoft Office

Job description

Medtronic Maastricht is seeking a Clinical Research Associate to monitor investigations at sites, ensuring adherence to protocols, regulatory requirements, and Medtronic procedures. You will work closely with study management teams and site staff to resolve issues and ensure smooth conduct of clinical studies.

You will collaborate with investigators, CROs, and research institutions to support initiation and advancement of clinical studies, review adverse events, and monitor timelines and