Senior Clinical Research Associate – Onsite Monitoring

IQVIA LLC in the United Kingdom is seeking a site management/monitoring professional to oversee the progress of assigned studies, including regulatory submissions, recruitment, CRF completion and data query resolution. The role requires coordinating with study teams, maintaining TMF/ISF in line with GCP and local requirements, and producing visit reports and follow-up letters.

A Bachelor’s degree in a scientific discipline or healthcare is preferred, with on-site monitoring experience.

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