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Clinical trials coordinator
| Posting date: | 10 April 2025 |
|---|---|
| Salary: | £44,806.00 to £53,134.00 per year |
| Additional salary information: | £44806.00 - £53134.00 a year |
| Hours: | Full time |
| Closing date: | 24 April 2025 |
| Location: | London, SE1 9RT |
| Company: | NHS Jobs |
| Job type: | Contract |
| Job reference: | C9196-25-0646 |
Summary
Are you adynamic and motivated clinical trial coordinator? Are you keen to coordinate clinical research thats embedded in a busy NHS setting? Are you organised and a great team player? This role will offer the post holder an opportunity to work closely with experienced clinical and research colleagues from across the trust, supporting a varied portfolio of non-commercial research studies. Successful candidates will be brilliant at communication with a range of teams and professionals, able to manage their time well and confident in research governance. Previous clinical research experience is essential. You will be joining an enthusiastic, friendly, and motivated multidisciplinary team in a dynamic teaching hospital in central London, and you will be an essential member of the research team. Role includes: Invoicing and financial oversight management Research governance and maintaining GCP Coordinating and managing studies in setup from feasibility to end of study Implementing and managing amendments to existing studies. Feasibility assessment and support local C&C assessment Organising Site Initiation Visits Overseeing study close down and managing archiving Supporting the research delivery team Overseeing procurement and ordering of consumables Acting as main a point of contact for enquires relevant to trial set up. Facilitating governance project board meetings on a monthly basis to discuss new research proposals. Updating EDGE/EPIC with recruitment when needed Confirming recruitment for sponsored studies on CPMS Playing a pivotal role in the monitoring and development of current local Standard Operating Procedures to ensure that they are fit for purpose and accurately detail procedures for study processes. Providing guidance and expertise on research set up, through development of specialist, in-depth knowledge. Working with the Principal Investigators, Research delivery team, R&D and management to ensure the successful set up of new studies. Supporting and guidance to new staff as appropriate in all area of study delivery/governance and provide training where necessary Providing regular updates on the progress of new studies Managing and prioritise their own workload Going through the researcher checklist handbook with new researchers Organisation of Investigator site file prior to sponsor greenlight including version control, localisation, signed delegation logs. Co leading the patient Research Advisory Group There are excellent opportunities for further education and leadership development within this role, including training and an individual personal development plan. The normal working hours for the post are9am-5pm but this can be discussed and there are opportunities for flexible working arrangements. The posts are mainly based at Guys Hospital but there will be cross site travel required to other sites such as St Thomas Hospital.