IQVIA Biotech in the United Kingdom seeks an experienced Clinical Research Associate to perform on-site monitoring across oncology studies. You will ensure protocol adherence, data integrity, and regulatory compliance while maintaining strong communication with sites.
The role requires 3–4 years of monitoring experience, a scientific/healthcare degree, and proficiency with MS Word/Excel/PowerPoint. This is a site-based position with accountability for recruitment tracking and site management in
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Senior CRA: Oncology Trials Lead & Site Impact 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.
