IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining TMF/ISF and liaising with the study team.
The role requires at least 2 years of on-site monitoring experience, solid knowledge of GCP/ICH, and excellent English communication.
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Lancashire
Join IQVIA on our mission to accelerate innovation for a healthier world!
South East
Join IQVIA on our mission to accelerate innovation for a healthier world!
Manchester, Lancashire
Join IQVIA on our mission to accelerate innovation for a healthier world!
Slough, Berkshire
Join IQVIA on our mission to accelerate innovation for a healthier world!
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