Tigermed is seeking a seasoned Clinical Research Associate in the United Kingdom to oversee site management, training, and documentation across studies. The role ensures compliance with ICH-GCP and regulatory requirements while coordinating study materials and EC submissions.
The ideal candidate has a bachelor degree or higher in medical/biology fields, at least 8 years of CRA experience, and strong MS Office skills.
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Manchester
Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials…
West of England
Tigermed is seeking an experienced Clinical Research Associate to lead site management for UK trials.
Wollaton
Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across…
Berkshire
In this role you lead Local Study Teams at country level to deliver study commitments on time and with quality, aligning with Sponsor procedures and…
London
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West of England
Study site selection, initiation (SIV) and clinical monitoring.
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