Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety Serve as primary Sponsor point of contact for investigative sites Train and motivate site staff and principal investigators on trial goals and patient treatment Conduct site evaluations, monitoring, training, and site closure with adherence to GCP/ICH and Manage site engagement strategies, report progress, and measure impact Ensure data quality and timely safety reporting; participate in risk assessment and site issue