IQVIA Biotech is seeking an on-site Monitoring professional to ensure high-quality conduct of oncology protocols and regulatory compliance across assigned sites. You will train and support site staff, manage recruitment plans, and coordinate with the study team to drive project success.
The role requires 1 year of CRA experience, strong knowledge of GCP/ICH guidelines, and excellent communication and organizational skills in English.
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CRA II – Oncology Site Monitoring & Trial Execution in Manchester 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.
