IQVIA Biotech is seeking a dedicated On-site Monitor to support oncology trials in the UK. You will conduct site visits, ensure protocol and regulatory compliance, and coordinate with study teams to drive enrollment and data integrity.
You will train site personnel on study procedures, track progress, and maintain essential TMF/ISF documentation while collaborating with cross-functional groups to meet project objectives in a fast-paced environment.
CRA II: Oncology Site Monitoring & Trial Oversight in Reading 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.
