Job Description

Globus Medical seeks a Clinical Research Associate to monitor and support clinical study sites for musculoskeletal research. The role ensures participant safety, data integrity, and regulatory compliance across remote and on-site activities while serving as liaison between sponsor and investigational sites.

Responsibilities

• Conduct site qualification, initiation, interim monitoring, and closeout visits in compliance with protocols and regulations
• Review source documentation, verify study data, and evaluate protocol compliance across assigned sites
• Monitor enrollment, retention, data quality metrics and identify site performance issues for resolution
• Support development and review of study documents including case report forms, informed consent forms, and EDC systems
• Maintain productive relationships with investigators, site personnel, and internal stakeholders to support study execution

Requirements

• Bachelor's degree in scientific, healthcare, engineering, or related discipline
• 1-3 years clinical research experience in medical device, biotech, or pharma industry
• Working knowledge of GCP and clinical research regulations
• Strong organizational, analytical, and problem-solving skills
• Proficiency with Microsoft Office; EDC or CTMS experience preferred
• Ability to travel up to 70% of the time
• Excellent verbal, written, and interpersonal communication abilities

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