Tigermed is seeking an experienced Clinical Research Associate (CRA) in the United Kingdom to manage study sites, oversee site initiation and monitoring, and ensure compliance with protocol and ICH-GCP. You will coordinate study materials, training, and regulatory submissions to EC and maintain trial documentation.
The role requires a Bachelor degree in a related field, 8+ years CRA experience, and strong knowledge of GCP and clinical trial operations.
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Senior Clinical Research Associate – UK (Site 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.
