Moorfields Eye Hospital, London

About the Company

Moorfields is one of the world’s leading eye hospitals, providing expertise in clinical care, research and teaching and education.

Our main focus is the treatment and care of NHS patients with a wide range of eye problems, from common complaints to rare conditions, which require treatments not available anywhere else in the UK. We have over 30 locations in and around London, which enables us to provide expert treatment closer to patients’ homes.

We are also a postgraduate teaching centre and a national centre for ophthalmic research involving, with the UCL Institute of Ophthalmology, the largest ophthalmic research programme in the world.

In addition, we manage three commercial divisions: Moorfields Private, Moorfields Pharmaceuticals and Moorfields Eye Hospital Dubai.

With our partners at the UCL Institute of Ophthalmology, we are members of Vision 2020, an organisation committed to raising public awareness of blindness and vision impairment as major public health issues.

Listed Jobs

Company Name

Moorfields Eye Hospital, London

Job Title

Study Coordinator - Research & Development

Job Description

Job Title: Study Coordinator – Research & Development Role Summary: Provides administrative support to clinical specialty teams within a Clinical Research Facility, coordinating research activities, ensuring compliance with governance regulations, and managing data acquisition and entry. Expectations: Work flexibly to meet objectives and deadlines; demonstrate proactive initiative in procedure development; operate independently while prioritising workload; maintain confidentiality and adherence to information governance; complete a Good Clinical Practice (GCP) research governance training within 3 months if not already certified. Key Responsibilities: - Support research leads and specialty teams with day‑to‑day administrative tasks. - Acquire, verify, and enter research data into spreadsheets. - Conduct literature searches and manage research documentation. - Coordinate study logistics, including scheduling and participant tracking. - Ensure research activities comply with current governance and ethical standards. - Maintain accurate and confidential records. - Facilitate communication between clinical and administrative staff. Required Skills: - Experience in medical or clinical research administration. - Proficient in data entry, spreadsheet management, and internet research tools. - Strong secretarial abilities (organising files, correspondence). - Excellent organisational and prioritisation skills. - Ability to work independently and manage conflicting demands. - Commitment to confidentiality and information governance. Required Education & Certifications: - Minimum of a secondary education qualification; higher education (e.g., Bachelor’s degree in a relevant field) preferred. - Completion of a Good Clinical Practice (GCP) research governance training course is required within 3 months of appointment.

London, United kingdom

On site

26-11-2025