Job Description

Medtronic seeks a Clinical Research Specialist to support neurovascular clinical studies across multiple sites. The role manages site operations, regulatory documentation, data quality, and compliance with clinical protocols and GCP requirements.

Responsibilities

• Manage clinical study sites through activation and closeout phases, including training and issue resolution
• Review and maintain regulatory and study documentation to ensure site activation and ongoing compliance
• Coordinate investigator and site staff activities to ensure protocol adherence and data quality
• Review clinical data, resolve discrepancies, and track open queries with study monitors
• Prepare reports on clinical investigation progress, milestones, and study results

Requirements

• High school diploma plus 6+ years, or associate's degree plus 4+ years, or bachelor's degree plus 2+ years of clinical research or clinical operations experience
• Clinical study site management and clinical research support experience
• Knowledge of Good Clinical Practice (GCP) requirements and compliance
• Ability to review clinical data, resolve discrepancies, and maintain study documentation
• CCRA or SOCRA certification preferred
• Medical device clinical research experience preferred

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