We are looking for a detail-oriented and process-driven individual to join our team in a support role focused on clinical trial documentation and task coordination . The primary responsibility of this role is to build electronic taskpads —structured lists of trial-specific tasks that guide clinic teams through protocol requirements. Each clinical trial is unique, so the taskpads must be tailored accordingly. This involves reviewing clinical trial protocols and accurately translating the trial schedule into a clear, actionable task list. Key Responsibilities: Review clinical trial protocols to create customised electronic taskpads Ensure all tasks align with the specific requirements and timelines outlined in each protocol Support the team by updating electronic records following protocol amendments Maintain up-to-date documentation and ensure relevant stakeholders are informed of any changes Work closely with clinic and trial operations teams to ensure accuracy and compliance About You: Strong attention to detail and a methodical approach to task management Ability to interpret technical documents (e.g. clinical trial protocols) Excellent communication and coordination skills Comfortable working with electronic systems and managing data Prior experience in clinical trials, healthcare, or research environments is a plus, but not essential This is a great opportunity to play a vital role in the smooth execution of clinical trials, ensuring processes are followed accurately and efficiently.
