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Opportunity 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 timeline...
  • Full time Life Scientists

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