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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Contract CRA UK - Site Lead & Trial Oversight 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.
