Tigermed is seeking an experienced Clinical Research Associate (CRA) to manage site initiation, monitoring, and data collection across studies in line with protocol and regulatory standards.
The role requires strong knowledge of GCP and trial operations, with responsibility for site qualification, training, and supplier coordination. You will monitor safety reporting and ensure compliant documentation throughout trial conduct.
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Contract CRA – UK: Site Management & Study 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.
