To support a global clinical program, the fully remote Clinical Research Associate will conduct site selection, monitoring, and close-out visits for various clinical trials while ensuring compliance with regulatory standards and driving patient recruitment strategies.
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 enhance patient recruitment, enrollment, and retention strategies to meet study goals Monitor site performance and protocol compliance, implementing corrective actions to maintain 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 Proven ability to manage investigative sites and ensure high standards of data quality and patient safety Proficiency in Microsoft Office and clinical trial management systems