CRA II — Oncology Site Monitoring in Biotech

IQVIA Biotech in the United Kingdom seeks an on-site Clinical Research Associate to monitor oncology studies and ensure GCP/ICH compliance. You will coordinate with sites, manage recruitment plans, and maintain high-quality study documentation.

You will train site staff, communicate regularly with investigators, and assist with study start-up activities while supporting regulatory submissions and data management. A scientific or healthcare degree and English proficiency are required.

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