Clinical Research Associate: Impact-Driven Trial Monitoring

NML Medical; Lower Providence Township (PA); On-site; USD 70,000 - 95,000; Full time

Job summary

Globus Medical seeks a Clinical Research Associate to monitor and support clinical study sites, ensuring participant safety and data integrity. You will qualify, initiate, monitor, and closeout sites per protocols and regulatory standards, acting as a liaison between sponsor and sites.

Travel up to 70% may be required. The role requires 1–3 years in clinical research, familiarity with GCP and applicable regulations, and strong communication skills.

Qualifications

• Bachelor's degree in a scientific, healthcare, engineering, or related discipline; equivalent combination of education and relevant clinical research experience may be considered.
• Excellent verbal and written communication; ability to collaborate across functions.
• 1–3 years of clinical research experience, including site monitoring in medical device, biotech, or pharma.

Responsibilities

• Conducts remote and on-site monitoring, including qualification/initiation, interim monitoring, and closeout visits per SOPs and regulations.
• Review source documentation and verify data, escalate issues and adverse events.
• Monitor site enrollment, retention, protocol compliance, and data quality; support site performance improvements.
• Ensure compliance with GCP, FDA ISO 14155, EU MDR, and sponsor requirements.
• Maintain relationships with investigators and study staff; support study materials and tools development.

Skills

Communication skills

Organizational skills

Problem-solving

Travel readiness

Education

Bachelor's degree in scientific/healthcare field

Tools

EDC

CTMS

Job description

Globus Medical seeks a Clinical Research Associate to monitor and support clinical study sites, ensuring participant safety and data integrity. You will qualify, initiate, monitor, and closeout sites per protocols and regulatory standards, acting as a liaison between sponsor and sites.

Travel up to 70% may be required. The role requires 1–3 years in clinical research, familiarity with GCP and applicable regulations, and strong communication skills.