Clinical Research Associate 2 (CRA 2)
About this role
About the Role The Clinical Research Associate 2 (CRA 2) monitors and manages clinical trial sites to ensure adherence to study protocols regulatory requirements and guidelines. The role focuses on site management subject recruitment and data quality while maintaining clear communication with study teams and stakeholders. What You'll Do
- Conduct site monitoring visits including selection initiation monitoring and close-out visits in compliance with GCP and ICH guidelines.
- Work with sites to adapt drive and track subject recruitment plans in alignment with project needs to enhance predictability.
- Administer protocol and study-related training to assigned sites; establish regular communication to manage project expectations and address issues.
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