IQVIA Biotech is seeking a qualified Clinical Research Associate to perform on-site monitoring visits and manage site performance on oncology studies. You will ensure protocol compliance, site training, and timely regulatory submissions while maintaining strong communication with sites and the study team.
The role requires a minimum of 1 year in on-site monitoring, familiarity with GCP/ICH guidelines, and solid English communication skills.
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CRA II: Oncology Site Monitoring Specialist 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.
