To support a growing portfolio of clinical studies, the full-time Clinical Research Associate II will act as the primary liaison between investigational sites, sponsors, and project teams, ensuring compliance with ICH-GCP guidelines and maintaining high standards of patient safety and data quality. Key Responsibilities Build and maintain strong relationships with Principal Investigators, Study Coordinators, and site personnel Conduct site selection, initiation, monitoring, and close-out visits, performing both remote and on-site activities Ensure participant safety and protocol compliance while preparing monitoring reports and maintaining inspection-ready documentation Required Qualifications Degree in Life Sciences, Clinical Research, Nursing, Pharmacy, or a related field Strong understanding of ICH-GCP and clinical trial regulations Minimum of 2 years of independent monitoring experience in clinical trials on-site Excellent communication and relationship-building skills Strong organizational skills and ability to work independently while collaborating effectively