IQVIA Biotech seeks an on-site Clinical Research Monitor with oncology study experience to oversee site performance, protocol adherence, and data quality across trials in the United Kingdom. You will collaborate with investigative sites, manage recruitment plans, and ensure regulatory compliance throughout the study lifecycle.
The role requires a science/healthcare background, strong English communication, and proficiency with standard MS Office tools.
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Senior CRA, Oncology — Fast-Paced Biotech Impact employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
