Assessing, screening, and recruiting suitable patients/ and participants for research studies providing ongoing review of clinical trial participants and the delivery of clinical investigations and treatments, as defined by the clinical trial protocol. Obtaining informed consent where appropriate, ensuring participants understand the study, risks, and rights. Performing clinical procedures such as blood sampling, administering study medications, monitoring vital signs, and managing and recording side effects. Manages the patient schedule to ensure all observations, interventions and procedures are carried out in accordance with the trial protocol Acting as a patient advocate, ensuring safety and wellbeing throughout the study.
Ensuring compliance with ethical approvals, research governance, and legal requirements. Upholding confidentiality and data protection standards

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