Senior Clinical Research Associate

As a Senior CRA you will: Conduct and report all types of onsite monitoring visits. Be involved in study startup (if applicable). Perform CRF review, source document verification and query resolution. Be responsible for site communication and management. Supervise study activities, timelines, and schedules on the country level. Be a point of contact for in-house support services and vendors. Be involved in quality control, such as compliance monitoring and reports review. Participate in feasibility research. Support regulatory team in preparing documents for study submissions.