You will hold a degree in a relevant biomedical science or have equivalent experience, alongside a strong background in clinical trial management, coordination or monitoring. A clear understanding of ICH-GCP, research governance, and regulatory requirements for CTIMPs is essential, as is experience of working with clinical research databases and applying quality systems in practice. You should be able to demonstrate proven project management skills, excellent organisation, and the ability to work independently while meeting deadlines.
Your experience will include working with NHS staff or within NHS research settings, and you will be confident in liaising with investigators, research nurses, and multidisciplinary teams across multiple sites. You must be willing and able to travel nationally when required and possess strong communication and reporting skills, with the ability to analyse information, resolve problems, and maintain high standards of accuracy and compliance.