Position Overview
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 timeline...