IQVIA LLC is seeking a Clinical Research Monitor to oversee site monitoring and management, ensuring studies are conducted per protocol and regulatory requirements. You will perform site visits, support data reporting, and work closely with study teams to maintain quality and timelines.
The role requires at least 2 years of on-site monitoring experience, strong communication and organizational skills, and proficiency with MS Office. Visa sponsorship is not available for this position.
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Senior Clinical Research Site Monitor 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.
