Trial Manager in London inLondon PUBLISHED THU 12 JUN 2025 Jump to job information section

The post holder will have responsibility for leading a team which will be delivering important academic haematology cell therapy trials, including phase 1 CAR T cell and stem cell transplant trials.

The post holder will need to be able to work autonomously, including close monitoring and coordination of apheresis slots, cell manufacturing, trial protocols and ensuring trial governance and patient safety are prioritised. The post holder will be expected to lead overall study coordination- including coordination across different sites, trial costing and trial budgetary management.

The post holder will be a key member of the research team and contribute to the development of the service. The post holder will advise and support patients in relation to the research study, monitor patients' physical and emotional wellbeing, and report and act on any untoward side effects

Clinical responsibilities to include coordinate Academic trials at multi centre level and project manage participating study sites external to KCH for academic clinical trials

Ensure trials are managed within current UK clinical trial directives and regulations in accordance with ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the clinical trial protocol is adhered to at all times.

Team lead and staff management

Regulatory submissions and overall study management

About us

As a Trial Lead the post holder will need to attend clinic, wards and multi-disciplinary meetings to facilitate the patient pathway. Given the nature of the studies, and the complexities involved, the post will require an ability to co-ordinate and liaise with all members of the Haematology department, including both the in- and out-patient clinical service and additional support services such as stem cell laboratories, production scientists, research laboratories and apheresis units.

The post will also require liaison and coordination with external sites where the clinical studies will also be running. The post holder will also be responsible for compiling local Information packs and regulatory submissions. The post holder will also be required to perform remote or onsite source data verification for multi-centre projects