Are you driven by a passion for clinical research and a desire to make a difference in ophthalmology? We invite you to join our dynamic team as one of two Clinical Trial Ophthalmic Technicians for a groundbreaking, 12-month contract in Oxford, UK, focusing on retinitis pigmentosa. In this impactful position, you will collaborate closely with participants and researchers, conducting mobility maze assessments that evaluate the effects of cutting-edge gene therapy on individuals with visual impairments. This is your chance to contribute to meaningful change while refining your clinical research skills in an encouraging and collaborative environment. Key Responsibilities: Execute mobility maze assessments under the guidance of the Principal Investigator (PI), ensuring full compliance with trial protocols. Partner with the clinical trial team, including sponsors and study monitors, to facilitate effective and timely trial progression. Prepare trial materials and maintain the maze and related equipment to ensure participant safety and functionality. Keep comprehensive and precise records of trial activities and participant performance in line with regulatory standards. Report any Adverse Events (AEs) and Serious Adverse Events (SAEs) as required. Uphold Good Clinical Practice (GCP) and adhere to Standard Operating Procedures (SOPs). Engage in additional research-related duties during non-trial periods to enhance the study's success. Create a welcoming and supportive atmosphere for participants, particularly those aged 16 and older with inherited retinal dystrophy. Implement risk assessments and follow infection control protocols to ensure a safe environment for everyone involved. Champion safeguarding and welfare policies for vulnerable individuals, adhering to all relevant guidelines. Candidate Requirements: A strong interest in clinical trials, particularly within ophthalmology and visual sciences. Exceptional organizational and communication abilities, with a knack for independent and collaborative work. Flexibility in your schedule to accommodate participant needs between 08:00 and 17:00. Proficiency in IT and the secure management of sensitive information. Commitment to ICH-GCP guidelines. Strong verbal and written communication skills. Reliable personal transportation is essential. Previous experience in a healthcare setting is advantageous. What We Offer Hands-on experience in a trailblazing clinical trial. Training in basic first aid and additional essential protocols. A collaborative and nurturing work environment. An opportunity to contribute to pioneering research in gene therapy for retinitis pigmentosa. If you are self-motivated, detail-oriented, and eager to improve the lives of individuals with visual impairments, we encourage you to apply now Your work can make a transformative difference in this vital area of healthcare.