Tigermed is seeking an experienced Clinical Research Associate to oversee site initiation, monitoring and data quality across multiple studies in the UK. The role requires strong GCP knowledge, 8+ years of CRA experience, and proficient use of MS Office tools.
Travel to sites will be involved to ensure protocol adherence and timely data collection. Candidates should be comfortable coordinating with investigators, ensuring safety reporting timelines, and contributing to study documentation and
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Senior Clinical Trial CRA - Site Management & Safety 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.
