You should be educated to degree level (minimum 2:1) or have extensive experience in relevant roles, such as study management or coordination. A solid understanding of sponsor responsibilities, research governance, and regulatory guidelines for clinical research is essential, as is experience in managing ethical submissions for clinical studies. You should be comfortable using standard office systems, such as word processing and spreadsheets, and have excellent written and verbal communication skills.
We are looking for a self-motivated individual who can manage multiple priorities, solve problems creatively, and work effectively both independently and as part of a team. Experience in multi-centre trials and project management is crucial, and knowledge of medical or research terminology would be advantageous. A willingness to travel within the UK and work flexibly to meet study requirements is also essential.
If you are passionate about clinical research and ready to take on a leadership role in managing complex studies, we encourage you to apply for this exciting opportunity at the University of Leicester.