IQVIA Biotech in Reading, United Kingdom, is seeking an experienced On-site Monitoring Specialist to support oncology trials under GCP/ICH guidelines. You will manage site visits, oversee recruitment, and ensure regulatory compliance across_trial activities.
Ideal candidates have 3–4 years of on-site monitoring experience, a science or healthcare degree, and strong communication skills in English. The role emphasizes collaboration with study teams and site management within a global CRO
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Senior Clinical Research Associate – Oncology Monitoring in Reading 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.
