Clinical Research Associate-Jobs in Großbritannien

Applicants must be HCPC state registered and have demonstrable experience of working in a diagnostic Microbiology laboratory. The Department has over 60 staff and processes over 500,000 samples per year. It has UKAS accreditation and is recognised IBMS training laboratory. The applicant will rotate through all sections of the laboratory and the Molecular facility in UHP Estover. They will examine a wide range of clinical samples from patients to determine laboratory diagnosis and the appropriate treatment of infection due to bacteria, viruses, fungi or parasites. Staff are encouraged to further their own development and assist with CPD related activities. The laboratory is well equipped and fully computerised.

It is a full-time post 09:00-17:30 Monday to Friday; with extended working days (early 8am, core, late shifts up to 10pm and nightshifts from 10pm-8am). Participation in a weekend rota, bank holiday rota and on call once trained is expected. All weekend work is paid at an enhanced rate as per Agenda for Change.

For the applicants requiring sponsorship, please check the attached criteria to qualify.

To perform microbiological analysis of biological samples including blood, urine, faeces, cerebral spinal fluid and other clinical samples, taking personal responsibility for the quality of the results, which are used in the diagnosis, treatment and management of infectious disease, and the detection and monitoring of hospital and community-based outbreaks of infection.

Maintain a high standard of professional knowledge and competence in the performance of all tests and investigations carried out at bench level.

To make diagnostic decisions of infection and treatment options, based on microscopic findings, the analysis of bacterial culture plates, and the subsequent assessment of bacterial susceptibility tests, which requires in depth knowledge, experience, expertise and judgement.

When working alone at night or at weekends, eg. when on-call, to carry out essential investigations and make critical diagnostic decisions unsupervised, and with no on-site back-up or reference point.

To work, if required, with high-risk samples and cultures, at Containment Level 3, and to be aware when circumstances arise necessitating the move of normal laboratory investigations (Containment Level 2) to a higher containment level.

To have sufficient knowledge and competence to work on rotation in all bacteriology and serology sections of the laboratory as required.

About Us

We are a people business - where every member of staff matters and can make a difference. Patients are at the heart of everything we do. Joining University Hospitals Plymouth NHS Trust means becoming part of a team of dedicated staff, who are committed to leading the way through innovation, clinical excellence and great customer care.

PLEASE NOTE THAT ALL COMMUNICATION WILL BE ELECTRONIC, PLEASE CHECK YOUR EMAILS REGULARLY. If you have any issues with applying online and need additional support including reasonable adjustments with the application process, please contact the recruitment team on 01752 432100. We recognise that work life balance is important for our colleagues and so we invite requests from applicants around less than full time/flexible working for our advertised roles. Please contact the recruiting manager to discuss this prior to your application submission. We commit to giving this full consideration in each case. We encourage people from diverse backgrounds to apply for our roles, as diversity strengthens our teams. It is sometimes necessary to close vacancies before the closing date. If you have not heard from us within 4 weeks of the closing date, please assume that you have not been shortlisted.

*Preference will be given to internal Trust staff, as well as 'Priority' and 'At Risk' status including NHS At Risk staff throughout Devon who are able to display recent relevant experience as dictated by the Person Specification

Date posted: 24 September 2025

Pay scheme: Agenda for Change

Band: Band 5

Salary: £31,049 to £37,796 a year per annum

Contract: Permanent

Working pattern: Full-time

Reference number: 216-EG-C7442765

Job locations: Derriford Hospital / UHP Estover, Derriford Road, PLYMOUTH, PL6 8DH

To be prepared to train in the use of new and emerging techniques and procedures, eg. molecular. The post holder will demonstrate the high level of skill to perform complex manual, semi-automated and automated analytical techniques as applicable, meeting turnaround times with prompt reporting of results used in the diagnosis and treatment of disease. The post holder will be required to provide complex information relating to test results, which may be sensitive in nature. As a state registered Scientist with the Health Professions Council to understand the pathology of infectious disease in relationship to the results produced, with reference to the normal findings, whilst understanding their significance for patient treatment and welfare. Will be aware of the clinical significance of results produced and using this knowledge to perform appropriate supplementary tests/investigations relevant to providing a complete report to requesting clinicians. To prioritise work and perform urgent analyses, reporting results promptly to requesting clinicians as appropriate. Identify abnormal or unexpected results and ensure prompt reporting, follow up and referral to medical staff, and to other reporting bodies, as required. Following protocols, request additional tests or samples to aid in the diagnosis or treatment of disease. To understand the principles underlying the analytical processes used in your area of work so as to maintain their operation and quality of results. To receive request forms, and accompanying samples, to decide on the appropriate investigations by understanding and interpreting the clinical information provided, to prepare samples and reagents for analysis, inoculate culture medium and set up tests as required. Answer telephone enquiries regarding results and other general laboratory issues e.g. giving advice on the correct conditions and sample type for a particular test request. To operate analytical equipment within your section, within your discipline and within the department, some of which will be highly complex and require specialist training. To be aware of faults and problems that may occur in the day-to-day use of analysers and expensive automated equipment e.g. multichannel analysers. To participate in and understand the quality assurance programs of the department, both internal and external i.e. NEQAS (National External Quality Assurance Schemes). To observe all departmental, Trust, national and European Health & Safety regulations relevant to the service, ensuring attendance at the annual departmental H&S update. In addition all staff must sign the departmental H&S policy to acknowledge understanding and compliance. To continually update their knowledge and skills whilst documenting this in their Continuing Professional Development folder. To have a basic understanding of the departments computer systems, and to be able, if required to use Microsoft Word and Excel software. To assist senior colleagues in the maintenance of adequate stocks of reagents and consumables to ensure continuous service provision. To follow Standard Operating Procedures if appropriate, contribute to their formulation, and propose any changes, in order to maintain the quality of the service and maximise efficiency. To attend meetings and training courses as necessary. To attend Statutory and Essential Update Training annually. To assist in the process of continual quality improvement. This will include audit, corrective action, preventative action and improvement processes. To participate in an annual appraisal and achieve any targets set at this time. To participate in the training of Trainee Biomedical Scientists and new staff. To assist senior staff in the supervision of Trainee Biomedical Scientists and Assistant Technical Officers. To assist in audit carried out by the Quality Manager, internal and external agencies. As part of a team, contribute to the continuous improvement program of the Pathology service. Participate in clinical trials or any research & development undertaken by the department, including sample preparation, analysis and collating data as necessary. At the direction of senior departmental staff undertake work from any source commensurate with the knowledge and skills of a state registered Biomedical Scientist. Ensure issues and problems are resolved satisfactorily and referred through your line management structure as appropriate. Be prepared to work on your own when necessary. To assist in validation and verification of new tests and their write up. To carry out other duties commensurate with the post.