Clinical Research Nurse

at  North Tees and Hartlepool NHS Foundation Trust

We are seeking an enthusiastic, experienced Research Nurse to join our Research Team. The post holder will have responsibility for the day to day running of National Institute of Health Research (NIHR) portfolio clinical research studies initially within A&E including Trauma and Orthopaedics or GI and Hepatology. Experience managing research studies within the NHS is advantageous. You will be responsible for obtaining regulatory approvals, managing the implementation of research protocols and co-ordinating the recruitment of patients into portfolio studies to time and target and any resultant data collection and follow-up requirements.
Manage a portfolio for NIHR research studies from expressions of interest to archiving.
Liaise with clinical teams and support services to ensure the smooth set-up and delivery of research studies.
Support patients participating in research studies.
Ensure sound financial management of research studies.
At North Tees & Hartlepool NHS Foundation Trust our main priority is, and always will be, to provide safe and high quality care to our patients every day; the kind of care we would want for ourselves and our loved ones. We want our organisation to be the best place to work with the right staff, in the right roles, at the right time, to ensure we deliver exceptional patient care and experience.
We will support staff through providing an inclusive and supportive workplace with health and well-being initiatives, staff benefits and opportunities for personal and professional development. Staff recognition is very important to us; as well as performance reviews and appraisals, we recognise staff through Star and Team of the month, colleague recognition a note of thanks, Managers Awards, Shining Stars and Service Awards.
We recruit for values and Together we are North Tees & Hartlepool
Organise and co-ordinate the set-up of NIHR portfolio research.
Evaluate patient eligibility for clinical trials, co-ordinating pre-study tests, obtaining results and arranging appropriate appointments according to trial protocol.
Ensure that you are working according to principles of ICH GCP and the EU Clinical Trial Directive and adhere to Research Governance standards for clinical research.
Act as a resource and support to patients and their carers explaining practical aspects of research studies. Work with clinical teams to map the patient pathway for each trial.Arrange collection of any samples required as part of the study and ensure safe and appropriate processing and storage of specimens.
Liaise with members of the MDTs. Pharmacists, Radiologists and Pathologists to establish procedures for the safe and smooth running of clinical trials.
To maintain accurate records ensuring that confidentiality of information is adhered to.
Assist in the review of trial protocols and identify resource implications for the site. This will involve assisting with the negotiation of financial agreements and contracts and ensuring departments are reimbursed as per agreement.
To co-ordinate the completion of submissions for local ethical and R&D approval and ensure other legislative requirements are met as required
To be responsible for the collection, co-ordination and computerisation of data generated from portfolio studies and the accurate, timely completion of case report forms (CRFs

Please refer the Job description for details