Clinical Research Officer
| Company: | NHS Jobs |
|---|---|
| Salary: | £32,073 to £39,043 a year |
| Hours: | Full-time |
| Location: | Wakefield, WF1 3SP |
| Job type: | Contract |
| Posting date: | 21 Oct 2026 |
| Closing date: | 4 Nov 2026 |
Summary
JOB SUMMARY The NHS constitution (2009) includes a pledge to the promotion and conduct of research to improve the current and future health and care of the population. The Research and Development Department has the principle aim of increasing quality research activity which promotes a vibrant research culture within the Trust. This is achieved through delivering and facilitating high quality research, providing support and advice on research methodologies, supporting the generation of research income through external sources and fostering collaboration with other trusts, universities, research bodies and the National Institute for Health Research (NIHR). The NIHR is funded through the Department of Health to improve the health and wealth of the nation through research. The NIHR Clinical Research Network (CRN) is the clinical research delivery arm of the NHS and there are 15 CRNs across England. The CRN: Yorkshire and Humber is hosted by Sheffield Teaching Hospital NHS Trust. The CRN is structured into 6 research divisions covering 30 clinical specialties. The post holder will work predominantly on studies within the mental health and dementia and neurodegenerative disorders (DeNDRoN) specialities. A temporary Clinical Research Officer (1 WTE) is required to work with clinicians and other specialists to manage and coordinate studies included in the NIHR CRN portfolio, these predominately being observational studies and some clinical trials. Adhering to Trust policies and procedures and the research protocol and ensuring support, care and safety of those involved in the trials. Their main areas of work will focus on: 1. Assessing feasibility of potential new CRN portfolio studies 2. Setting up new CRN portfolio studies 3. Ensuring the first participant is recruited into the study within specified timescales 4. Ensuring recruitment targets are achieved within specified timescales for each study 5. Increasing the number of research active staff For a limited period, pending full implementation of Health Research Authority Approval, the post holder will also be required to coordinate aspects of Research Governance for some studies with support from the Research Administrator and supervised by the Research and Development Manager. This will include processing studies not currently eligible for HRA approval through the existing NHS Permission process, processing study amendments and providing advice on and support for Research Governance to local clinicians and researchers. Travel across Trust sites and occasional out of hours working will be required. KEY RESULT AREAS: Each study will be at a different stage of the research process and specific tasks undertaken by the Clinical Research Officer will vary according to the nature of each study and as detailed in the protocol. Key tasks for each stage are outlined in 1-5 below: 1. Feasibility and study set up Link closely with Trust services to identify opportunities for new research Assess the feasibility of new portfolio studies with the Principle Investigator and under the supervision of the Research & Development Manager, by reviewing the protocol, assessing any resource implications and seeking specialist advice where required. Working with the Research & Development Manager and Principle Investigator calculate an achievable recruitment target for the study and set up timelines which will ensure the first patient can be recruited by target date. Assist the Research & Development team in undertaking the costings for commercial research projects. In collaboration with the Research & Development Manager and Principle Investigator develop an appropriate recruitment plan to address potential recruitment barriers and to ensure patient awareness and any education needs are met, seeking advice from service users and carers in the Research Involvement Group where appropriate. Liaise with the Research & Development team, the Principle Investigator and the study team in order to assist with the completion of local site specific information forms and the localising of participant documents. Organise project feasibility and site initiation meetings, staff training and co-ordinate any resource requirements, e.g. room bookings and equipment. Circulate study information and deliver study presentations to promote the research locally. 2. Recruitment and screening Meet regularly with the local Principal Investigator and other clinicians to identify eligible participants, increase study awareness, provide study information and updates, identify any areas of low recruitment and increase recruitment. Screen potential study participants using, for example the study inclusion and exclusion criteria and Trust clinical system RiO. Prepare invitation letters on behalf of clinicians. Ensure study specific investigations and screening tools are undertaken as required by the protocol to establish eligibility and safety to enter the study. Monitor participants condition throughout the study, including monitoring of any adverse events and ensure changes to treatment as required by the protocol. Report and record (serious) adverse events that occur whilst the participant is in the clinical trial [study] to the trial coordinator/Principle Investigator and relevant local personnel/regulatory authorities within agreed timescales. Obtain clinical specimens (including bloods) from participants, store and package them according to the research protocol and organise their safe and timely delivery to the appropriate laboratory. Open and maintain an accurate record of each study within the Local Portfolio Management System (currently EDGE) and maintain an accurate local record of each participant screened and recruited into the study. Ensure the data on the NIHR CRN Open Data Platform (ODP) accurately reflects the local record by maintaining close communication with the study team and report any inconsistencies to the CRN team. Make home visits or clinic visits in order to take informed consent and complete study specific data collection. Where patients lack capacity to consent, or there is doubt around capacity, ensure appropriate liaison with clinicians and compliance with appropriate legislation and guidance. Respect participant confidentiality at all times and protect the confidentiality of any personal information. 3. Data collection and storage Encourage retention of participants throughout the study by providing ongoing communication and support to participants and clinicians. Complete follow up visits either in participant homes or clinics. Be responsible, under the guidance of the Principal Investigator, for the collection, anonymisation, storage, organisation and transfer of project data. Ensure the accuracy and completeness of data collected. Collect and despatch biological samples e.g. saliva or blood, that may be required for the study, according to protocol (training will be provided where appropriate). Undertake study specific and routine assessments e.g. vital signs, ECG, height/weight measurements, as well as safely deliver medication and explain use according to an agreed protocol, take bloods and order investigations in line with research protocol (training will be provided where appropriate and there will be no requirement for the postholder to interpret the findings or make clinical decisions, e.g. ECG results etc). Administer payments to participants, keeping accurate logs and receipts to support accurate and timely invoicing. Record and report any adverse events in accordance with the study protocol and ICH -Good Clinical Practice and EU Directives. Communicating with appropriate personnel and regulatory authorities within agreed timescales. Conduct risk assessments as required by the study protocol/SOPs and in conjunction with Trust reporting requirements. Ensure prompt completion of any follow up actions, seeking guidance when required. 4. Management of the study Ensure effective liaison with relevant staff, internal and external to ensure the smooth running of the study in accordance with the latest approved protocol, ICH-Good Clinical Practice and any study specific or R&D Standard Operating Procedures. Maintain the study site file in accordance with ICH-Good Clinical Practice. Review the impact of any study amendments and liaise with study team to ensure the amendment is implemented effectively. Facilitate and prepare for audit/monitoring visits that may be conducted by R&D staff, study sponsor and contract research organisation. Adhere to ICH-Good Clinical Practice standards, the Research Governance Framework (DH 2005), national Regulatory requirements (Data Protection Act, Mental Capacity Act, Human Tissue Act, EU Directives) and Trust policy. Ensure effective liaison with teams within the Trust, including, Information Governance, Medical Records, Clinical Governance, Practice Effectiveness, Training and Development, Patient Safety and Risk and Mental Health Act Office. Maintain accurate study costs and liaise with finance to ensure timely and accurate invoices are raised and full study costs are recovered where appropriate. Ensure effective liaison with external research associated organisations including NIHR CRN, Academic Health Science Network, Research Design Service, Clinical Trials Unit, Sponsor, Contract Research Organisation, University partners and Health Research Authority. For full details of the role please see the supporting documents attached. All employees of the Trust are strongly encouraged to have their up-to-date flu vaccination to protect staff and patients. We are aware that an increasing number of applicants are using AI technology to generate responses on NHS Job application forms. We strongly discourage this and will conduct a thorough screening process before selecting candidates to progress to the next stage. If you are using AI to enhance your application, please disclose this in your application form.