Remote Clinical Research Associate

To support a global clinical program, the fully remote Clinical Research Associate will conduct site selection, initiation, monitoring, and close-out visits for various clinical trials while ensuring compliance with regulatory standards and driving patient recruitment strategies. Key responsibilities Conduct site visits for clinical trials, ensuring compliance with GCP, ICH, and regulatory standards Partner with investigative sites to enhance patient recruitment, enrollment, and retention strategies Monitor site performance and implement corrective actions to maintain data integrity and patient safety Required qualifications Bachelor's degree in Life Sciences, Healthcare, Nursing, Pharmacy, or a related field preferred Minimum of 3 years of recent on-site clinical monitoring experience with relevant therapeutic areas Strong knowledge of GCP, ICH guidelines, and FDA regulations Demonstrated ability to manage investigative sites and ensure protocol compliance Proficiency in Microsoft Office and clinical trial management systems