Part Time Research Nurse

• Remain fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, timelines, and relevant SOPs
• Communicate with the Illingworth research nurse project manager, Research nurse manager, site staff, and Principal Investigator
• Maintain accurate documentation and electronic data transfers while ensuring subject confidentiality, GCP, and data protection compliance
• Attend Site Initiation Visits and other required meetings
• Coordinate and complete subject trial visits on- and off-site with the RN team
• Complete trial procedures and assessments according to protocol and SOPs and collect accurate data
• Administer trial medication and facilitate its safe storage, transfer, and accountability
• Process, package, and dispatch samples while liaising with courier companies and organizations
• Assist with identifying eligible patients and patient recruitment into clinical trials
• Provide patient information and support for on- and off-site care
• Report adverse events, serious adverse events, and SUSARs to the site team and RNPM
• Report suspected misconduct or fraud to Illingworth and associated companies

• Registered nurse with a minimum of 2 years' post qualification experience
• Research and clinical trials experience with GCP certification
• Knowledge of research design and methodology desirable
• Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable
• Ability to work autonomously with initiative in a team within a multidisciplinary environment
• Excellent verbal and written communication skills
• Ability to prioritize and manage multiple tasks
• Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum
• Equivalent experience, skills, and/or education will also be considered

• Part-time employment
• Remote work (pre-approved)