Clinical Research Associate (cra) – Oncology Studies (6+ Months) - Sponsor Dedicated - Türkiye
IQVIA UK
Türkiye
Oncology studies monitoring
Site selection and initiation
Gcp and ich guidelines
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
Job Summary
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.
Evaluate the quality and integrity of site practices related to protocol compliance, patient safety, and regulatory adherence; escalate quality issues when necessary.
Collaborate effectively with cross‑functional study team members to support overall project delivery.
Matching Summary
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.