Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, with 8+ years of CRA experience and strong MS Office skills.
Responsibilities include SIV, site initiation, monitoring, and ensuring compliance, safety reporting, budget finalisation, and timely study materials coordination.
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West of England
Tigermed is seeking an experienced Clinical Research Associate to lead site management for UK trials.
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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.
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Study site selection, initiation (SIV) and clinical monitoring.
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Study site selection, initiation (SIV) and clinical monitoring.
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