IQVIA Biotech in Reading is seeking an experienced Clinical Research Associate to monitor oncology sites, ensuring GCP/ICH compliance and robust data quality. You will manage regulatory submissions, site training, and TMF documentation while coordinating with study teams.
The role emphasizes proactive enrollment tracking, site relationship management, and accurate study documentation within IQVIA's global clinical research network.
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Senior CRA – Oncology On-site Monitoring Expert in Reading 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.
