IQVIA Biotech is seeking a dedicated on-site monitor to support oncology studies in the Reading area. You will conduct site visits, drive patient recruitment plans, and ensure protocol training with clear communication to sites and stakeholders.
The role requires 1 year of on-site monitoring experience and a solid understanding of GCP/ICH guidelines, with strong English communication and organizational skills. Collaboration with the study team is essential to ensure timely trial progression.
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Oncology Clinical Monitoring Specialist (CRA II) 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.
