Clinical Research Associate II: Site Monitoring & Studies
IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol training, TMF/ISF maintenance, data query resolution, and collaboration with the study team to ensure quality and timely delivery.
Applicants should have a Bachelor's degree in a scientific discipline or healthcare, at least 1 year of on-site monitoring
As a Clinical Research Associate II:
Site Monitoring & Studies, you will play an important part at IQVIA in Reading, England, United Kingdom.
We are seeking a motivated Clinical Research Associate II:
Site Monitoring & Studies to join IQVIA in Reading, England, United Kingdom.
Consider building your career as a Clinical Research Associate II:
Site Monitoring & Studies at IQVIA.
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