IQVIA Biotech is seeking an on-site Clinical Site Monitor to support oncology studies in the UK. You will conduct monitoring visits, ensure compliance with GCP/ICH, and liaise with sites to drive patient recruitment and data quality.
The role requires a Bachelor’s degree in a scientific field, 1–2 years of on-site monitoring experience, and strong English communication. UK right to work is required.
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CRA II: Oncology Clinical Trials (UK) in Livingston 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.
