Tigermed in Cambridge, United Kingdom, is seeking a qualified Clinical Research Associate to oversee site management, initiation, and monitoring for multiple studies. You will ensure safety reporting, regulatory compliance, and efficient study administration.
The role requires strong knowledge of ICH-GCP, trial operations, and extensive experience with MS Office tools. You will collaborate with site staff to ensure protocol adherence and timely study completion.
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UK Contract CRA: Site Management & Trial Oversight in Cambridge 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.
