Tigermed in the United Kingdom is seeking an experienced Clinical Research Associate (CRA) to manage sites, initiate studies, and monitor trials in compliance with protocol and regulatory requirements.
The role requires at least 8 years of CRA experience, strong knowledge of ICH-GCP, and proficiency in Word, Excel, PowerPoint and Outlook. You will coordinate study materials, budgets, and site submissions while maintaining trial master files.
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Contractor CRA - Site & Study Management (UK) in Nottingham 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.
