The Role
1. Responsible for the patients taking part in the study
2. Ensuring study compliance in relation to the ICH-GCP
3. Maintain patient records inclusive of patient’s response to the trial and effectively reporting adverse events as per protocol, providing medical treatment to all patients as required
4. Complete tasks as delegated by the Principle Investigator
5. Manage the clinical trial as required, providing adequate guidance, training and mentoring to ensure that the study is completed to the higher standard, to protocol and fully compliant.
You
6. Valid and in date GMC registration with no restrictions
7. Must have completed FY1 and FY2 in an NHS setting, plus additional clinical experience
8. Experience of working within a clinical research setting preferred but not essential
9. Able to work collaboratively with the wider clinical research team
10. Complete all required training as needed to carry out clinical trials