Post-Doctoral Research Scientist
Listed on 2026-08-06
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Research/Development
Research Scientist, Clinical Research, Medical Science
This post is a fixed term/secondment for 12 months to meet the needs of the service. If you are interested in applying for the secondment position, you must obtain permission from your current line manager prior to applying for this post. The Component Development and Research (CDR) Laboratory performs development and research activities on blood components, with the aim to improve clinical outcomes of transfusion and the manufacture of blood components as well as contributing to scientific research in this field.
This is a technical and scientific role, responsible for delivering innovative research and evaluation projects under the direction of the Head of Department within Component Development and Research. The post holder will be required to develop and perform complex assays on the quality and function of blood components using specialist equipment, in addition to manufacturing novel blood components for research projects.
You will be expected to lead the development of research studies, grant-funding applications and disseminate research findings through presentations, peer reviewed publications and reports, as well as be involved in exploring research and development opportunities with external collaborators.
- The post holder will be expected to lead in the production of peer reviewed publications, including posters, abstracts and presentations.
- Design and lead research and development projects with and without supervision.
- Generate projects for students at both undergraduate and postgraduate level and act in a technical supervisory role in association with the student's academic body.
- Source and complete grant funding applications for research projects,
- Experience of post-graduate research at a doctoral level
- Experience of working in either a clinical or a research laboratory
- Significant wet laboratory experience
- Experience of verbal and written communication of complex information
- Experience of training others in laboratory methods and supervising implementation of new processes
- Experience of planning experiments to meet project objectives and delivering work within set timelines
- Experience of writing academic publications in the life sciences
- Experience of analysing and interpreting large and complex datasets
- Knowledge of research methods
- Knowledge of Good Practise Guidelines
- Experience of manufacturing blood components
- Demonstrable experience of optimising and validating either manufacturing technologies or testing platforms and adapting new technologies
- Experience of working within a regulated environment (e.g. ISO 9001, GLP, UKAS, MHRA)
- Experience of conducting research and evaluation in transfusion medicine field
- Experience of contributing to external funding applications
- Clear verbal communicator with good scientific report writing and presentation skills.
- Capable of constructing and delivering clear ideas and complex information
- Ability to analyse and interpret scientific data, pre-empt and evaluate issues and recommend appropriate course of action
- Ability to work independently and within a team.
- Can work on own initiative, is self-motivated, organised and meticulous
- IT literate & willingness to develop IT skills using various software packages
- Generic Laboratory skills e.g. pipetting, microscopy etc
- Planning and organisational skills and ability to prioritise work and work to deadlines
- Self-confident, motivated and reliable
- Proven ability to take a leading role on multidisciplinary projects and ability to interact with external partners on fast paced projects Willing to travel overseas e.g. to conferences
- Welsh is desirable at level 1
- Knowledge of QMS inc. change control, CAPA & incident reporting, An interest in evidence-based medicine and practise
- A desire to deliver high quality work
- Proactive approach to tasks
- Respectful of other people's opinions and ideas
- Flexible and creative, continuously improving
- Able to take responsibility for own work
- Ability to be flexible in hours worked in accordance with exigencies of the service
- Awareness of the Velindre NHS Trust Values
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