Clinical Research Associate II

Job Summary

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