Clinical Research Nurse
| Dyddiad hysbysebu: | 29 Ebrill 2026 |
|---|---|
| Cyflog: | £17.00 i £20.00 yr awr |
| Gwybodaeth ychwanegol am y cyflog: | £17.00 - £20.00 an hour |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 15 Mai 2026 |
| Lleoliad: | Thetford, IP24 2HY |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | M0038-26-0395 |
Crynodeb
Assist research manager to ensure the research team processes are maintained and developed. Assist in developing clinical research policies, procedures and SOPs. Screen, recruit, randomise and maintain research participants within studies. Co-ordinate own case load of clinical studies and participants. Ensure clinical trials methodology is adhered to. Ensure that work is carried out to ICH GCP, Research Governance and EU Clinical Trials Directive standards for all clinical studies. Undertake clinical procedures including collection and handling of biological samples. Act as primary point of contact for participants on a clinical study. Ensure all participants are managed safely according to surgery policies and guidelines. Take informed consent from participants where authorised. Liaise with external clinical study personnel as necessary. Supply data as required to the PI regarding progress of clinical studies. Identify barriers to recruitment and ensure PI is aware of them; identify and implement action plans to remove these barriers. Assist the doctors in monitoring the research participants condition throughout their time within the clinical trial. Ensure safe administration of treatments and drugs in the context of a clinical study. Ensure that the study specific investigations are undertaken as required by the protocol in order to establish eligibility and safety to enter the trial. Provide ongoing information, education and support to participants regarding the clinical trials. Maintain accurate documentation of research related activities in the study and surgery notes. Monitor treatment toxicity/ side effects and initiate changes to treatment as required by the protocol. Follow all local, network and sponsor policies and procedure to ensure you are working according to GCP and Research Governance standards for the clinical studies. Work within the NMC Code of Conduct and scope of professional conduct.