IQVIA is seeking a Senior Clinical Research Associate in the UK to join our Site Management team. You will perform site monitoring visits, support site recruitment plans, and ensure regulatory compliance across interventional studies.
The role requires 3–5 years of on-site monitoring experience, a degree in a scientific discipline or healthcare, and strong knowledge of GCP/ICH guidelines. Visa sponsorship is not available for this position.
Senior CRA I - On-Site Clinical Monitoring (UK) in Manchester employer: QPL IQVIA RDS Poland Sp. z o.o.
IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, where your contributions directly impact global health outcomes. With a strong emphasis on employee growth, you will have access to mentorship opportunities and professional development resources, all while working in a dynamic environment that values diversity and creativity. Located in a vibrant area, our team enjoys a supportive atmosphere that encourages meaningful work and personal fulfilment.
Contact Details:
QPL IQVIA RDS Poland Sp. z o.o. Recruitment Team
