IQVIA Biotech is seeking a dedicated On-site Monitor to support oncology trials in the UK. You will conduct site visits, ensure protocol and regulatory compliance, and coordinate with study teams to drive enrollment and data integrity.
You will train site personnel on study procedures, track progress, and maintain essential TMF/ISF documentation while collaborating with cross-functional groups to meet project objectives in a fast-paced environment.
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CRA II: Oncology Site Monitoring & Trial Oversight 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.
