**Job Overview**

Join our team as a Clinical Research Site Manager, where you’ll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements.

**Essential Functions**

+ **Site Monitoring:** Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
+ **Recruitment Management:** Collaborate with sites to develop, drive, and track recruitment plans, enhancing predictability and meeting project needs.
+ **Training & Communication:** Provide protocol training and maintain regular communication with sites to manage expectations and address issues.
+ **Quality Assurance:** Evaluate site practices for protocol adherence and escalate quality issues as needed.
+ **Study Progress:** Track regulatory submissions, recruitment, enrollment, case report form (CRF) completion, ...