Clinical Research Associate

Job Summary

To support a global clinical program, the Clinical Research Associate will conduct site selection, monitoring, and close-out visits for various clinical trials, ensuring compliance with regulatory standards in a fully remote position with travel across the U.S.

Key responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits for clinical trials, ensuring compliance with GCP, ICH, and protocol requirements
• Partner with investigative sites to drive patient recruitment and retention strategies, supporting study timelines and performance goals
• Monitor site performance and protocol compliance, identifying quality concerns and 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 with direct experience in Cardiovascular, CNS, Diabetes, and/or GLP-1 clinical trials
• Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes
• Demonstrated ability to independently manage investigative sites and ensure high standards of data quality and patient safety
• Proficiency in Microsoft Office and clinical trial management systems, with excellent organizational and relationship-building skills