**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 protocol an...