IQVIA Biotech in the United Kingdom seeks an on-site Clinical Research Monitor to oversee site visits, training and regulatory adherence. You will partner with study sites to optimize recruitment and data integrity, ensuring timely submissions and compliant conduct of oncology trials.
Ideal candidates bring 1–2 years on-site monitoring experience, strong English communication, and a solid understanding of GCP/ICH guidelines.
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Clinical Research Associate II – Oncology Monitoring, UK in Manchester 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.
