Job Overview:
The Clinical Research Associate 2 (CRA 2) is responsible for monitoring and managing clinical trial sites to ensure adherence to study protocols regulatory requirements and guidelines. The CRA plays a key role in site management subject recruitment and data quality while maintaining clear communication with study teams and stakeholders.
Responsibilities:
Conduct site monitoring visits including selection initiation monitoring and close-out visits in compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (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.Evaluate the quality and integrity of site practices to ensure proper conduct of the study...