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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CRA II — Oncology Site Monitoring in Biotech employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
