Clinical Research Associate

Job Summary

To support a global clinical program, the full-time Clinical Research Associate will conduct site selection, monitoring, and close-out visits for various clinical trials while working remotely with some travel required.

Key responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits for clinical trials, ensuring compliance with GCP, ICH, and regulatory standards
• Partner with investigative sites to enhance patient recruitment, enrollment, and retention strategies aligned with study goals
• Monitor site performance and protocol compliance, implementing corrective actions to ensure data integrity and patient safety

Required qualifications

• Bachelor's degree in Life Sciences, Healthcare, Nursing, Pharmacy, or a related scientific discipline preferred
• Minimum of 3 years of recent on-site clinical monitoring experience in relevant therapeutic areas
• Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes
• Demonstrated ability to independently manage investigative sites and maintain high data quality standards
• Proficiency in Microsoft Office and clinical trial management systems