The JRO is handling an unprecedented number of queries, applications and contracts, affecting the speed of throughput and response to queries. Read more on how queries and applications will be processed.
Find out if your study requires a sponsor and approvals and permissions you need before you start. Access JRO support in regulatory advice, study set-up, NHS feasibility, contracting, PPI, statistics and IMP management.
The JRO has produced Standard Operating Procedures guidance documents, and templates for UCL/UCLH investigators and research staff, governing the management and operational aspects of conducting clinical research.
The JRO supports researchers at UCL/H in the set-up and oversight of clinical research studies. The growing portfolio of high quality research aims to improve the lives of patients and the care provided.
Have a quick question or require some guidance? Refer to our frequently asked questions which covers topics ranging from IRAS applications through to funding, research passports and who to contact at the JRO.