IQVIA Biotech in Reading is seeking an on-site Clinical Research Associate to join a fast-paced team. You will perform site monitoring visits, ensure regulatory compliance, and support site recruitment and data management across oncology studies.
You will coordinate with site staff, train investigators, and maintain essential study documentation, including TMF/ISF, while upholding GCP and ICH standards. This role offers a clear career path within a global CRO focused on biotech partnerships.
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Oncology CRA II: Site Monitoring & Trial Coordination 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.
