Tigermed is seeking an experienced Clinical Research Associate to oversee site management, initiation visits and ongoing monitoring across selected sites in the UK. The role focuses on ensuring protocol adherence, staff training, and timely safety reporting in line with ICH-GCP and sponsor SOPs.
You will coordinate site selection, oversee documentation, and manage budgets and study materials while ensuring regulatory submissions and trial master files are up to date throughout the study
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Contract CRA: Site Management & Trial Start-Up in Bournemouth 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.
