IQVIA is seeking a Senior Clinical Research Associate for its CFSP model in the UK, including Livingston. You’ll conduct site visits, ensure data integrity, and train site staff within a sponsor-dedicated CFSP framework.
The role requires 2+ years of on-site monitoring experience and a strong knowledge of GCP/ICH, with travel up to 40–60%. Join a global organization with ongoing professional development, cross-functional collaboration, and opportunities to advance in clinical research across
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Senior CRA: Global Clinical Trials & Site Leadership in Livingston 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.
