**IQVIA Türkiye is looking for** **an** **Experienced Clinical Research Associate (CRA)** **to join our growing clinical operations teams. The ideal candidate will have** **a minimum of 6 months of hands-on experience in oncology studies** **and will play a key role in ensuring the successful execution of clinical trials in compliance with applicable regulations and sponsor requirements.**

**Key Responsibilities**

+ Perform monitoring and site management activities to ensure that clinical trial sites conduct studies and report data in accordance with the study protocol, applicable regulations, and sponsor requirements.
+ Conduct site monitoring visits including **site selection, initiation, routine monitoring, and close‑out visits** in line with contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
+ Work closely with sites to adapt, drive, and track subject recruitment plans to support project timelines and predictability.
+...