Remote Clinical Research Associate

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 efforts. 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 implement patient recruitment and retention strategies that align with study timelines and performance goals Monitor site performance and protocol compliance, addressing quality concerns and maintaining 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 involvement in Cardiovascular, CNS, Diabetes, and/or GLP-1 clinical trials 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