IQVIA UK is seeking experienced Clinical Research Associates to join the cFSP team in the South West England. The role focuses on on-site monitoring, recruitment planning, regulatory compliance, and site training to ensure trial integrity and patient safety.
Candidates should have at least 2 years of independent monitoring experience in interventional studies, with knowledge of GCP/ICH and UK regulatory requirements.
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Clinical Research Associate - On-site Monitor in Bath 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.
