IQVIA in Reading, United Kingdom is seeking a Senior Clinical Research Associate (CRA) to lead on-site monitoring across PI sites within a cfSP framework. You will ensure patient safety, data integrity, and protocol adherence while building strong investigator relationships.
The role requires 4+ years of on-site monitoring in CRO/pharma settings, solid GCP/ICH knowledge, and the ability to travel up to 40–60% of the time.
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Senior CRA, CFSP Specialist – Global Trials 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.
