Clinical Research Associate

Responsibilities: of the Clinical Research Associate : • Conduct site qualification, initiation, routine monitoring, and closeout visits. • Ensure studies are conducted in compliance with ICH-GCP guidelines, protocols, and regulatory requirements. • Review source documentation, site records, and data for accuracy and compliance. • Build and maintain strong relationships with investigators and site staff. • Identify, document, and resolve site issues while supporting overall study execution. • Complete monitoring reports and follow-up documentation within required timelines. • Travel extensively to clinical research sites as required. Qualifications: of the Clinical Research Associate : • 2+ years of independent monitoring experience as a Clinical Research Associate. • Bachelor's degree in a scientific, healthcare, or related field preferred. • Strong knowledge of ICH-GCP guidelines and clinical trial regulations. • Experience within pharmaceutical, biotechnology, or medical device studies preferred. • Excellent communication, organization, and problem-solving skills. • Ability and willingness to travel frequently, including overnight travel. Compensation: for the Clinical Research Associate includes : • Pay Rate: 110k-125k/year • Comprehensive benefits package including medical, dental, vision, 401(k), and PTO • Direct-hire opportunity with long-term career growth Application Period : This job opens for applications on 10/23/2026. Applications for this job will be accepted for at least 30 days from the posting date.