The JRCO will address any queries or issues relating to research conduct as and when notified to them, either formally or informally, as applicable.
The JRCO will conduct random or triggered audits of research activity to ensure compliance with regulation, approved procedure and local compliance systems.
As the trial progresses (IMP internally sponsored trials only), the JRCO will support its management by ensuring that the monitoring performed is in accordance with its monitoring plan, and that the CI/PI complies with the sponsor’s instructions and study procedures.
There is also a requirement to send regular updates and routine reports to a number of interested parties throughout a trial, eg Trial Steering Committees and funders.
Resources
| Type | Where to find |
|---|---|
| Key contacts | JRCO |
| Useful links | NIHR Clinical Trials Toolkit - NIHR Clinical Trials Toolkit - NIHR Clinical Trials Toolkit - NIHR Clinical Trials Toolkit - |
| NIHR benchmark | Post NIHR 70-day benchmark |
| Process map links | This activity occurs in the recruitment stage: > ³Ô¹ÏºÚÁÏ as sponsor > ³Ô¹ÏºÚÁÏ College Hospital NHS Trust as sponsor > Commercial organisation as sponsor > Non-commercial organisation as sponsor |