Project Manager, Clinical Eye Research Centre

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 Job description Job 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