**Fixed Term Contract/ Secondment opportunity for 2 years**
Do you have a passion for research? Would you like to work in a state-of-the-art building amongst a budding team of researchers and scientists?
The Research and Development department at NNUH is growing and an exciting opportunity has arisen for a Research Study Officer to join a supportive and dynamic team to help us develop our service.The R&D team is busy! You'll be joining a team of 22, including 6 research study officers who together manage the set-up of around 90 studies at any one time. You could be supporting anything from a straightforward questionnaire-based project to a new drug intervention.
As Research Study Officer, you will be the 'go-to' person ahead of a study commencing - you will plan and organize all the finer details to ensure the smooth running of studies once active.
Our ideal candidate will be self-motivated and able to confidently build relationships with a range of colleagues internally and externally, also enjoy a varied workload and be able to deliver results within set targets and strict deadlines.
** If you are considering applying for this post on a secondment basis, please discuss with your Line Manager prior to applying to ascertain whether this could be supported **
Full time: 37.5 hours per week.
Interview date: 11th April 2025.
As a study officer you will be responsible for the facilitation of study feasibility, set up, approvals and ongoing research management for research studies taking place at NNUH. This will include tracking the status of studies from pre-approval to completion by reference to a comprehensive data and financial management system. You will monitorrecruitment into studies, identifies studies which require support with recruitment processes, investigate and resolve problems, and provide data to inform decisions about the allocation of service support costs. You will liaise with investigators to ensure that study files contain all documentation, as required by Good Clinical Practice (GCP), before a study can commence.
You will be responsible for ensuring that the approval of new studies and protocol amendments is achieved in accordance with national regulatory frameworks and set timelines.
The study officer will work closely with the Grants Co-Ordinator, Research Governance Co-Ordinator and the Commercial Research Co-Ordinator providing advice to researchers and investigators on clinical research management, regulation and governance so they will need a strong working knowledge in this area.
The following skills and experience will be required and are essential for the successful candidates:
Please see attached Job Description for full details.
Please note that this advertised position, which is part of occupation code 2434 does not meet the UKVI eligibility requirements for a Skilled Worker Visa. The Trust would not be able to issue a Certificate of Sponsorship for this role unless you meet the 'new entrant' criteria or have continually held one or more Skilled Worker visas prior to 4 April 2024.