IQVIA Biotech is seeking an experienced Clinical Trial Monitor focused on on-site activities and Oncology studies. You will conduct site visits, ensure protocol compliance and regulatory adherence, and support site recruitment and data integrity across multiple sites.
The role requires 3–4 years of on-site monitoring experience, strong English communication, and solid knowledge of GCP/ICH guidelines. This position is not visa-sponsored and offers a dynamic, fast-paced environment within IQVIA
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Senior Oncology CRA — Advanced Site Monitoring Lead 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.
