IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to perform on-site monitoring visits, ensure GCP/ICH compliance, and support site start-up and ongoing study execution. You will collaborate with investigative sites, manage data and regulatory documentation, and help drive subject recruitment to meet project timelines.
The role requires 18 months of independent on-site monitoring, flexibility to travel, and a life science background.
Senior CRA - Frontline Clinical Trial Monitoring in the UK 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.
