IQVIA UK is seeking an Experienced Clinical Research Associate in Netanya, Israel, to perform site monitoring and management tasks in compliance with study protocols, regulations, and guidelines. The position requires at least two years of on-site monitoring experience and a strong understanding of clinical research regulatory requirements
Job Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Matching Summary
Match Score: 85
IQVIA UK is seeking an Experienced Clinical Research Associate in Netanya, Israel, to perform site monitoring and management tasks in compliance with study protocols, regulations, and guidelines. The position requires at least two years of on-site monitoring experience and a strong understanding of clinical research regulatory requirements.