Please note for this role you will be required to travel independently around the county meeting strict time deadlines. You will need to hold a full UK driving licence* and have use of a vehicle. You cannot use public transport for this role as this is not a reliable form of transport and will not allow you to meet service needs. Please confirm in your application that you meet the specified criteria.
Please refer to the attached job description and person specification for full details of responsibilities To support the delivery of the NETp project within CAMEO Cambridge and Peterborough NHS Foundation Trust. To identify potential participants from CAMEO Cambridge and Peterborough NHS Foundation Trust. To collate, collect and input participant questionnaire data To collect questionnaire and qualitative interview data from clinicians (and service users participants if required) in EIP services To develop and maintain effective contacts with EIP and relevant stakeholders To attend and contribute to appropriate multi-disciplinary meetings, steering groups and other forums as appropriate. To communicate information about studies and make presentations to clinicians and other relevant groups.
To ensure patients / carers are provided with written information relevant to the research study and are given the opportunity to discuss the research study or clinical trial adequately at the outset and during the course of the research or clinical trial in which they are being asked to participate (i.e. informed consent). To assist clinicians in taking consent from patients/participants to enter research studies. To provide information/reports on recruitment as requested by the regional PI and the NETp study management team.
Maintain regular contact with clinical teams participating in studies to encourage recruitment. To work at all times according to Good Clinical Practice and Trust Research Policy, and Trust SOPs. To ensure that any data collection is conducted according to specific research protocols (in liaison with the research teams) and adheres to the Data Protection Act 1998 and according to Good Clinical Practice guidelines. Adherence to and interpretation of research study protocols and standard operating procedures including compliance with local, national and international research regulations.
To assist participants with the completion of questionnaires as necessary. Maintain accurate patient trial documentation, complete Case Record Forms, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes. To carry out timely and accurate recording and storage or study data into study databases and storage system, maintaining data protection and GCP requirements at all times. Coordinate treatment, assessment and follow-up as necessary in accordance with research protocol.
To attend and support patients in the clinical environment for monitoring, assessment and follow up as part of research projects. Ensure safety data is reported to required SOPs and study protocols, and reports send in a timely manner. To record and report any adverse events and serious adverse events according to trial protocol and local procedures. *DVLA have a number ofreciprocalarrangements with overseas countries, for further information please visit the DVLA websit

Please refer the Job description for details