Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK, with access to world-class training and professional development
Job Summary
Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK, with access to world-class training and professional development.
Responsibilities include performing site monitoring visits, managing study progress, evaluating site practices, and creating documentation in accordance with GCP and ICH guidelines.
The role requires a minimum of 18 months of independent on-site monitoring experience and a life science degree or equivalent industry experience.
Matching Summary
Join IQVIA cFSP (sponsor-dedicated) as an experienced Clinical Research Associate in the UK, with access to world-class training and professional development.