IQVIA is hiring for an on-site Clinical Research Associate to monitor sites for oncology studies in Manchester. You will ensure adherence to GCP/ICH guidelines, manage site communications, and support recruitment planning and data integrity across multiple sites.
The role requires 3–4 years of monitoring experience, a scientific/healthcare degree, and strong English communication. Familiarity with TMF/ISF, regulatory submissions, and study documentation is essential.
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Senior Oncology CRA — Site Monitoring & Study Oversight 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.
