Clinical Research Associate
Current- Ensure Good Clinical Practice (GCP) compliance and accurate data verification.
- Perform routine monitoring visits, manage data queries, and ensure the integrity of trial data.
- Oversee the execution of monitoring plans, preparing reports, and resolving site issues.
- Provide site training and support.
- Facilitate technology support and ensure sites have access to necessary materials and information.
- Effective communication abilities to convey complex information clearly and liaise between site staff and the research team