Tigermed is seeking an experienced Clinical Research Associate to drive site management, training and safety reporting across multiple studies. You will coordinate SIVs, monitor visits, and ensure compliance with ICH-GCP and protocol requirements while maintaining trial master files and essential documents.
The role demands strong communication, budgeting, and documentation skills to manage sites, payments and study tools. On-site work in the UK is expected with occasional travel.
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Senior CRA – UK, Site Management & Monitoring in Wakefield 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.
