Tigermed is seeking an experienced CRA to oversee site management, initiation visits, monitoring, and compliance with ICH-GCP and regulatory requirements in clinical trials. The role covers study planning, site training, and coordination of essential trial materials.
Responsibilities include ensuring safety reporting, documenting visits, and maintaining trial master files. The ideal candidate has 8+ years CRA experience and strong proficiency in MS Office tools.
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Senior Contract CRA (UK) - Site Monitoring & Start-up in Slough 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.
