The post holder will provide essential administrative support to both clinical and non-clinical staff within the practice, working in close collaboration with the research team. This role involves supporting research nurses and clinicians to ensure that all administrative processes related to clinical trial such as screening, assessments, follow-ups, and data collection are carried out in an efficient and timely manner. The post-holder will develop good working relationships with: Research Nurses / Teams Wider practice team Patients participating in clinical research External clinical trial sponsors and providers Key Responsibilities: Support the coordination and preparation of clinical trial activities, particularly patient study visits. Assist with patient recruitment, data entry, and portfolio management. Ensure compliance with all clinical trial protocols and administrative procedures. Maintain accurate records and documentation associated with trial procedures. Collaborate with research nurses and clinical staff to support the delivery of the operational aspects of trial implementation. Liaise with patients, providing clear communication and administrative support throughout their participation in research studies. Other Responsibilities: Raise invoices as required and assist in tracking income generated from clinical trials. Ensure all administrative research activities are conducted in accordance with Good Clinical Practice (GCP) guidelines. Efficiently interpret and follow complex study protocols and Standard Operating Procedures (SOPs) provided by relevant trusts or sponsors to ensure compliance with regulatory requirements. Monitor and provide timely updates regarding Expressions of Interest (EOIs) and study timelines to support Principal Investigators (PIs) and Research Nurses. Undertake any other duties relevant to the role, as agreed upon with the line manager.