IQVIA Biotech in the United Kingdom seeks a site monitor with 1–2 years of on-site monitoring experience, especially in oncology trials. You will ensure quality, compliance with GCP/ICH, and effective collaboration with clinical sites.
Your role includes coordinating site training, tracking recruitment, and maintaining TMF/ISF documentation, with potential involvement in start-up and contract-based financial tasks. English proficiency is essential.
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CRA II: Oncology Trials Monitoring & Site Oversight 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.
