IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor and manage study sites, ensuring adherence to protocol, GCP/ICH guidelines, and regulatory requirements. The role involves site visits, recruitment support, training, and timely data logistics.
Applicants should have a scientific or health care degree and at least 1 year on-site monitoring experience. No UK visa sponsorship is available for this position.
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Manchester
Escalate quality issues as appropriateManage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and…
Langley
IQVIA LLC is seeking an on-site monitoring professional to ensure adherence to GCP and protocol requirements across multiple sites.
Langley
IQVIA is hiring an experienced Clinical Research Associate in the UK to conduct on-site monitoring visits and support study execution.
Bath
In this role you support the execution of interventional studies as a Clinical Research Associate within IQVIA's sponsor-dedicated team.
Reading
In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data.
Berkshire
In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data.
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