Tigermed is seeking an experienced Clinical Research Associate to lead site management for UK trials. You will oversee site selection, SIV initiation, monitoring, safety reporting, and study logistics to ensure protocol adherence and regulatory compliance.
You will train site staff on ICH-GCP, maintain trial master files, manage budgets and payments, and coordinate study tools and materials across sites. Strong MS Office skills and 8+ years CRA experience are required.
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Wollaton
Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across…
Manchester
Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials…
Normanton on Trent
Tigermed is seeking a seasoned Clinical Research Associate in the United Kingdom to oversee site management, training, and documentation across…
West of England
Study site selection, initiation (SIV) and clinical monitoring.
Manchester
Study site selection, initiation (SIV) and clinical monitoring.
Wollaton
Study site selection, initiation (SIV) and clinical monitoring.
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