**We are looking for Experienced Clinical Research Associates** to join our team and support the successful execution of clinical trials by performing high‑quality monitoring and site management activities. In this role, you will ensure that study sites operate in compliance with protocols, GCP/ICH guidelines, regulatory requirements, and sponsor expectations while maintaining strong communication and collaboration with site staff and internal teams.

**Responsibilities**

+ Conduct selection, initiation, monitoring, and close‑out visits according to GCP, ICH guidelines, and the contracted scope of work.
+ Work with sites to develop and track subject recruitment plans aligned with project timelines.
+ Provide protocol and study‑specific training to site personnel; maintain regular communication to support expectations and resolve issues.
+ Assess site performance and ensure adherence to protocol, study procedures, and regulatory compliance; escalate quality is...