Clinical Research Associate (CRA) – Oncology Studies (6+ Months) - Sponsor dedicated - Türkiye

Job description

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. - Deliver protocol, study‑specific, and ongoing training to investigative sites and maintain regular communication to manage expectations and address issues. - Evaluate the quality and integrity of site practices related to protocol compliance, patient safety, and regula...