Clinical Research Associate

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A Clinical Research Associate (CRA) plays a key role in the development and approval of new medicines and treatments. They coordinate and monitor clinical trials, ensuring studies are conducted ethically, safely, and according to regulatory standards. CRAs are responsible for checking clinical sites, collecting trial data, and ensuring that all protocols are followed. They often work for pharmaceutical companies, contract research organisations (CROs), or within the NHS. The position involves regular travel to trial sites, attention to detail, and strong communication skills, as CRAs act as a link between sponsors, medical staff, and regulatory bodies.

Clinical Research Associate

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