Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

Medtronic Clinical Research Solutions (MCRS) combines clinical research and evidence generation teams to support the successful execution of clinical studies across a range of therapies and technologies. The MCRS Monitoring team works directly with investigational sites to support patient safety, protocol compliance, and data integrity throughout the clinical trial lifecycle.

This role supports clinical trial activities through site monitoring, study coordination, and regulatory documentation management. The position requires regular travel to investigational sites and collaboration with internal study teams, investigators, and research personnel to support compliant and efficient study execution.

This entry-level clinical research role is responsible for supporting and monitoring clinical studies to ensure compliance with study protocols, Good Clinical Practice (GCP), regulatory requirements, and ethics committee policies. The individual will work closely with study teams and investigational sites to support trial conduct, site training, documentation review, and study operations activities.

Primary Responsibilities

• Conduct on-site and remote monitoring visits in accordance with study and monitoring plans.
• Review study conduct, source documentation, and trial data to support protocol and regulatory compliance.
• Identify and escalate protocol deviations, data discrepancies, and compliance issues.
• Prepare monitoring reports, follow-up communications, and study documentation within required timelines.
• Serve as a point of contact for investigational sites and support issue resolution with study teams.
• Support site initiation, training, and ongoing education for investigators and research staff.
• Assist with Ethics Committee submissions, Clinical Trial Agreement processes, invoices, and payment activities.
• Collaborate with cross-functional teams to support study execution and site performance.

Required Qualifications

• Clinical research monitoring or clinical trial support background.

• Ability to travel up to 75% and hold a valid driver's licence.
• Knowledge of Microsoft Word, Excel, PowerPoint, and database applications.
• Ability to work within cross-functional and matrix-based environments.

• Knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, Food and Drug Administration (FDA) regulations, International Organization for Standardization (ISO) standards, or clinical research regulations.

Preferred Qualifications

• Understanding of medical terminology and healthcare environments.
• Experience supporting Ethics Committee or Competent Authority submissions.
• Knowledge of clinical trial operations and study documentation processes.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

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Benefits & Compensation

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.
 

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