IQVIA Biotech in the United Kingdom seeks an on-site Clinical Research Associate to monitor oncology studies and ensure GCP/ICH compliance. You will coordinate with sites, manage recruitment plans, and maintain high-quality study documentation.
You will train site staff, communicate regularly with investigators, and assist with study start-up activities while supporting regulatory submissions and data management. A scientific or healthcare degree and English proficiency are required.
CRA II — Oncology Site Monitoring in Biotech employer: QUK IQVIA Ltd.
As a Dedicated Line Manager at our organisation, you will thrive in a supportive and dynamic work culture that prioritises employee development and collaboration. We offer comprehensive training programs, opportunities for professional growth, and a commitment to maintaining high standards in clinical research, all within a location that fosters innovation and teamwork. Join us to make a meaningful impact in the healthcare sector while enjoying a rewarding career path.
