Job summary
- Main area
- Ophthalmology Research
- Grade
- Band 6
- Contract
- Fixed term: 3 years (3 year contract from start date)
- Hours
- Part time - 23 hours per week (3 Weekdays TBC, office hours 8.30-5)
- Job ref
- 287-CEF-245-26
- Employer
- Liverpool University Hospitals NHS Foundation Trust
- Employer type
- NHS
- Site
- Royal Liverpool University Hospital
- Town
- Liverpool
- Salary
- £39,959 - £48,117 per annum
- Salary period
- Yearly
- Closing
- 31/07/2026 23:59
Employer heading
Project Manager, Clinical Eye Research Centre
Band 6
Job overview
The Clinical Eye Research Centre within Ophthalmology at the Liverpool Foundation Trust is a purpose built unit facilitating Clinical Trials and studies in all aspects of Eye Research. The unit undertakes and delivers clinical trials/studies in patients and healthy volunteers for commercial, non-commercial and sub contract studies.
This is an exciting opportunity to those with research background/knowledge to play a key role in a team working at the heart of ophthalmic research in the Liverpool City Region.
Main duties of the job
The successful candidate will possess excellent communication and interpersonal skills, demonstrate adaptability within a fast-paced and evolving environment, and bring a proactive, solutions-focused approach to their work.
The post holder will have primary responsibility for the operational coordination and delivery of the GREEN Study, for which Liverpool serves as the Chief Site. Acting as the principal point of contact for participating sites, sponsors and key stakeholders, the post holder will provide leadership and oversight to ensure successful study delivery and achievement of recruitment, governance and project milestones.
Working closely with the Chief Investigator, Principal Investigators, research teams, sponsors, university partners and external organisations, the post holder will coordinate study set-up, site support, regulatory submissions, project monitoring, financial oversight and risk management throughout the lifecycle of the GREEN Study.
When capacity allows and service needs require, the post holder will also provide support to the Clinical Eye Research Centre Business Team (CERCBT) in the coordination and management of other research studies and research-related business activities.
Working for our organisation
Liverpool University Hospitals NHS Foundation Trust comprises Aintree University Hospital, Broadgreen Hospital & Royal Liverpool University Hospital.
We are part of NHS University Hospitals of Liverpool Group, formed on 1 Nov 2024 from the coming together of LUHFT and Liverpool Women’s NHS Foundation Trust. The Group was born from a shared aim to improve the care we provide our patients.
UHLG is one of the largest employers in the region, with over 16,800 colleagues dedicated to caring for our communities - from birth and beyond.
For the 630,000 people across Merseyside, we are their local NHS. We provide general and emergency hospital care, alongside highly specialised regional services for more than two million people in the North West.
Aintree University Hospital is the single receiving site for adult major trauma patients in Cheshire and Merseyside and hosts a number of regional services including an award-winning stroke facility. Broadgreen Hospital is home to elective surgical, diagnostic and treatment services, together with specialist patient rehabilitation. Liverpool Women’s Hospital specialises in the health of women and babies, delivering over 7,200 babies in the UK’s largest single site maternity hospital each year. The Royal Liverpool University Hospital is the largest hospital in the country to provide inpatients with 100% single bedrooms and focuses on complex planned care and specialist services.
For roles at Liverpool Women’s, visit their careers page.
Detailed job description and main responsibilities
With support and mentorship from the Clinical Eye Research Centre Business Team (CERCBT), the post holder will take primary responsibility for the day-to-day operational management and coordination of the GREEN Study, ensuring that study objectives, recruitment targets, timelines, governance requirements, and sponsor expectations are achieved.
As Liverpool is the Chief Site for the GREEN Study, the post holder will act as the central point of contact for participating sites, providing advice, guidance, and administrative support throughout the lifecycle of the study. The post holder will work closely with the Chief Investigator, Principal Investigators, sponsors, partner organisations, and participating research sites to ensure effective study delivery.
The post holder will:
- Coordinate and oversee all operational aspects of the GREEN Study from set-up through to study completion.
- Act as the primary liaison between Liverpool and participating sites, ensuring clear communication, consistency of processes, and adherence to study requirements.
- Lead completion of study feasibilities, Expressions of Interest, study set-up documentation, and governance submissions associated with the GREEN Study.
- Prepare, coordinate, and oversee Ethics, Research & Development (R&D), regulatory, and sponsor submissions in conjunction with the Principal Investigator and research team.
- Develop, maintain, and monitor project plans, timelines, milestones, and study metrics, ensuring that delivery remains on track and corrective actions are taken where required.
- Coordinate cross-site activities and facilitate effective collaboration between research teams, sponsors, ancillary departments, and external stakeholders.
- Identify, document, monitor, and escalate project risks, ensuring appropriate mitigation plans are implemented and reviewed.
- Monitor study performance, recruitment targets, financial activity, and key deliverables, reporting progress to the study leadership team and sponsors as required.
- Establish and maintain effective working relationships with sponsors and collaborating organisations, ensuring a high standard of study management and stakeholder satisfaction.
- Coordinate and lead study meetings, preparing reports, updates, and presentations for internal and external stakeholders.
- Ensure monitoring visits, monitoring reports, and study documentation are completed, maintained, and actioned within agreed timescales.
- Support budget monitoring, invoicing processes, and financial reporting associated with the GREEN Study in collaboration with the RD&I Business Team.
- Ensure that all study activities are conducted in accordance with Good Clinical Practice (GCP), ICH guidelines, Trust policies, Standard Operating Procedures (SOPs), and regulatory requirements.
In addition to their responsibilities for the GREEN Study, the post holder will provide support to the Clinical Eye Research Centre Business Team on other non-commercial and commercial research studies as required, contributing to wider service objectives, project delivery, and operational resilience across the research portfolio.
The post holder will undertake any other duties commensurate with the grade of the post and as reasonably requested by management
Person specification
Qualifications
Essential criteria
- Graduate with Hons Degree/equivalent knowledge , preferably in a science or clinical area
- Relevant clinical research experience in a pharmaceutical company/CRO including study management and/or project management experience
Experience
Essential criteria
- Demonstrable experience in managing or coordination of clinical studies
- Experience in effective use of Microsoft Office package including Microsoft Project or other planning software
Desirable criteria
- Experience of liaison with staff at all levels in the NHS, Universities and Industry
- Leadership/management experience
- Experience of being a client/sponsors primary point of contact
- Experience in Phase I Clinical Trials
Knowledge
Essential criteria
- Knowledge of the principles & practice of clinical research and/or clinical trials
- Knowledge of ethical and quality standards applicable to clinical trials, including EU Directive ICH/GCP requirements
- Demonstrate knowledge of NHS Research Governance
- Ability to understand and work with financial information
- Working knowledge of study/trial management processes
Skills
Essential criteria
- Good communication, presentational, training and interpersonal skills
- Skills in administration & research management
- Ability to meet tight deadlines and cope in a highly demanding environment
- Ability to work independently and prioritise/own workload and to communicate effectively with all members of the multidisciplinary team
- Ability to liaise with clients/sponsors in a professional manner
- Good planning and organization skills
Desirable criteria
- Skills in handling and management of computerised data
- Skills required to evaluate and assist in developing new protocols
- Skills in the analysis and interpretation of data
Other
Essential criteria
- Meticulous attention to detail and a high standard of accuracy
- Flexible approach to working hours/days
Applicant requirements
The postholder will have access to vulnerable people in the course of their normal duties and as such this post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service to check for any previous criminal convictions.
Application numbers
Documents to download
Further details / informal visits contact
- Name
- Lindy Gee
- Job title
- Clinical Eye Research Centre Business Manager
- Email address
- [email protected]
- Telephone number
- 015 706 3873
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