Clinical Research Practitioner


Company:	NHS Jobs
Salary:	£47,951 to £56,863 a year
Hours:	Full-time
Location:	Denmark Hill, SE5 9RJ
Job type:	Contract
Posting date:	21 Oct 2026
Closing date:	4 Nov 2026

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Summary

Main Duties and Responsibilities 1. Assist in the process of gaining and maintaining all appropriate regulatory approvals associated with the conduct of the clinical study and other related high-quality clinical studies. 2. Responsible for recruiting to and following up participants within the study and other clinical studies and trials in the rheumatology research portfolio. 3. Ensure written informed consent has been obtained for any treatment provided for, or any data collected from a participant, which will form part of a research study, in accordance with the Trust research governance arrangements and The International Conference on Harmonisation of Good Clinical Practice (ICH GCP) Guideline. 4. Undertake study related tasks and procedures as required for the project, ensuring that they are carried out within the study protocols, Trusts policies, research governance guidance, the International Conference on Harmonisation of Good Clinical Practice (ICH GCP) Guideline and the Data Protection Act. 5. Act as a patient advocate, enabling patients to make informed choices concerning their involvement in the clinical trial and other related high quality clinical studies, and ensure appropriate advice and information is provided. 6. Evaluate research protocols and participant information materials and ensure that information about studies is clearly and appropriately communicated to research participants. 7. Undertake collection and management of study participant data (qualitative and quantitative). 8. Undertake training and maintain competency to use relevant equipment as per study protocols, eg. centrifuges. 9. Maintain all data and case report forms relating to the clinical trial and other high quality clinical studies in accordance with The International Conference on Harmonisation of Good Clinical Practice (ICH GCP) Guideline. 10. Analyse clinical data related to the trial and other related high quality clinical studies, working under the supervision of the Principle and Chief Investigators and other members of the wider research study team. 11. Work within the organisational policies and Standard Operating Procedures (SOPs) of the Trust and create procedures and SOPs as required for each research study. 12. Assist the Principle Investigator and other members of the study team in managing incidents, accidents and complaints in accordance with Trust policies and procedures. 13. Participate in audit of research procedures and processes as required. 14. Ensure all study documents are kept up to date, version controlled and effectively stored and archived as required. 15. Maintain an up-to-date knowledge of research related topics particularly related to qualitative studies. 16. Always communicate effectively and work to maintain a harmonious working environment. 17. Attend and organise meetings, workshops and conferences as agreed by the Chief or Principle Investigators and members of the wider research study team. 18. Effectively communicate research findings to different audiences, including patient and public contributors. 19. Be responsible for maintaining own competency through continuing professional development activities, including peer review, reflective practice, maintenance of a personal portfolio and attendance at specialist training courses/ events and local / national meetings as agreed with the Chief Investigator and members of the research study team. 20. Participate in regular performance appraisal meetings. 21. Provide training for students / others working on relevant research projects as appropriate. 22. Act as a role model by participating in group meetings and activities, showing a commitment to achieving results, encouraging and supporting other members of the team and patient and public involvement contributors and raising suggestions for continuous improvement 23. Any other duties appropriate to the post and grade that may be reasonably requested.

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