Tigermed is seeking an experienced Clinical Research Associate in the United Kingdom to oversee site management, training, documentation, and safety reporting across multiple studies. The candidate will coordinate SIVs, ensure regulatory compliance, and support budget and contracting activities.
Proficiency in MS Office and GCP is essential. The role requires strong organizational skills, attention to detail, and the ability to manage study materials and systems efficiently within a busy
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Senior UK CRA Contractor – Clinical Trials Lead in Chesterfield 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.
