Clinical Research Assistant

Job Overview

The NIHR Moorfields Clinical Research Facility (‘CRF’) is a purpose‑built facility that supports world‑class experimental ophthalmic research to translate scientific advances into benefits for patients. Patients and volunteers visiting the CRF can take part in research programmes safely and effectively according to robust, ethically approved protocols. The Clinical Research Assistant will work under the direction of the clinical research nursing team to provide clinical and administrative support for the delivery of clinical research studies.

• Participate in the delivery of patient care
• Contribute towards department organisation
• Venepuncture after successful training and supervision
• Collection, processing, storage and shipping of biological samples; give support to the clinical research team in the provision of a safe and caring environment
• Assist with the induction and supervision of new staff undertaking this role
• Work as a supportive and versatile team member

The Clinical Research Assistant will demonstrate a level of skill and understanding which enables them to take responsibility for specific tasks delegated by the nurse in charge in accordance with agreed policies and procedures.

• To develop research awareness through in‑house training and completion of Good Clinical Practice training.
• To attend appropriate research meetings.
• Assist in the coordination, organisation and implementation of basic science and clinical trial protocols in accordance with International Conference on Harmonisation/ Good Clinical Practice (ICH/GCP). This will include complex commercial trials.
• Using appropriate manual and computerized systems, ensure accurate collection and maintenance of all research records and results.
• Assume day‑to‑day responsibility for specific research studies as delegated by the Senior Research Nurse.
• Assist in the development and implementation of research study plans for delegated studies.
• Assist in the development of Standard Operating Procedures (SOPs), for use by all clinicians using the MEH CRF, both within and outside the unit.
• Facilitate effective communication of complex research study information with all relevant research personnel, including: medical, nursing, administrative and pharmacy staff.
• Assist in the development and implementation of research initiatives in liaison with other MEH CRF staff.

What’s in it for You?

At Moorfields, we invest in you—your growth, your wellbeing, your future.

• Competitive salary (including high‑cost area supplement)
• Membership of the NHS Pension Scheme
• 24/7 independent counselling support
• Career‑long learning and development opportunities
• Excellent transport connections
• Access to NHS and Blue Light discount schemes
• Free Pilates classes
• Full support and training to develop your skills

And so much more! To see the full range of benefits we offer please view our Moorfields benefits leaflet.

• To comply at all times with the requirements of the Health & Safety regulations under the Health & Safety at Work Act (1974) and to take responsibility for the health and safety and welfare of others in the working environment ensuring that agreed safety procedures are carried out to maintain a safe environment.
• To comply at all times with the Trust’s Data Security Policy. Also to respect confidentiality of information about staff, patients and health service business and in particular the confidentiality of electronically stored personal data in line with the Data Protection Act.
• The Trust has adopted a security policy in order to help protect patients, visitors and staff and to safeguard their property. All employees have a responsibility to ensure that those persons using the Trust and its service are as secure as possible.
• It is the responsibility of all trust employees to fully comply with the safeguarding policies and procedures of the trust. As a Moorfields employee you must ensure that you understand your role in protecting adults and children that may be at risk of abuse.…