Tigermed in the United Kingdom is seeking an experienced CRA to oversee site management, initiation visits, and ongoing monitoring per protocol and regulatory requirements. You will coordinate safety reporting, site training, and document control across multi-site studies.
Ideal candidates have a strong background in GCP, at least 8 years of CRA experience, and proficiency with MS Office tools. The role focuses on ensuring quality data and regulatory compliance throughout study conduct.
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Senior Clinical Research Associate (CRA) - UK | Site Monitoring in Coventry 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.
