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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Senior Clinical Research Associate, UK - Contract employer: Tigermed
As a fully remote employer in the pharmaceutical industry, we pride ourselves on fostering a collaborative and inclusive work culture that values communication and teamwork. Our employees benefit from extensive growth opportunities, including the chance to lead and establish teams within a global framework, all while enjoying the flexibility of remote work. Join us to be part of a dynamic environment where your expertise is valued and your contributions make a meaningful impact.
