IQVIA Biotech in the United Kingdom seeks an on-site Clinical Monitor to oversee trial sites, ensure GCP/ICH compliance, and manage data quality. The role emphasizes oncology study oversight and coordination with site teams.
Ideal candidates have 1–2 years of on-site monitoring experience, a science/healthcare degree, and strong English communication skills. UK right to work is required; visa sponsorship is not offered.
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CRA II: Oncology Trials Monitor in Fast-Pace Biotech 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.
