Clinical Research Monitor
About The Position
The Clinical Research Monitor is an entry-level role within Medtronic Clinical Research Solutions (MCRS), supporting and monitoring clinical studies across a range of therapies and technologies. The role helps ensure patient safety, protocol compliance, data integrity, and adherence to Good Clinical Practice (GCP), regulatory requirements, and ethics committee policies throughout the clinical trial lifecycle. The position works closely with study teams, investigators, and investigational-site research personnel to support site monitoring, study coordination, trial conduct, site training, regulatory documentation, and study operations. Regular travel to investigational sites is required, with travel of up to 75%.
Requirements
- Clinical research monitoring or clinical trial support background.
- Ability to travel up to 75%.
- 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.
Nice To Haves
- Understanding of medical terminology and healthcare environments.
- Experience supporting Ethics Committee or Competent Authority submissions.
- Knowledge of clinical trial operations and study documentation processes.
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.
Benefits
- Flexible benefits package
- Competitive compensation plans
- Short-term incentive through the Medtronic Incentive Plan (MIP)
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
