Job Description
We are looking for a research bioinformatician to work in the Royal Marsden BRC Translational Research team, supporting clinical trials and BRC-funded translational research projects. The post-holder will work with a highly experienced bioinformatics teams to develop pipelines to analyse paediatric cancer data primarily obtained with next generation sequencing using short (Illumina) and long read (Nanopore) sequencing platforms. The work will take place in the Clinical Genomics Translational Research Laboratory at The Centre for Molecular Pathology at The Royal Marsden NHS FT and The Institute of Cancer Research in Sutton. The postholder will join a team with an international track record in translating research to clinical practice for the benefit of patients. The primary role of the post holder will be to develop bioinformatic pipelines for BRC-funded translational research projects. This includes developing novel approaches to circulating cell free DNA (cfDNA) analysis for diagnosing paediatric cancer and monitoring treatment. Other workstreams include the use of long read sequencing for structural variant detection. They will also support the development of cross-BRC theme informatic solutions to enable direct transfer of genomic reports to electronic patient records and linkage to other healthcare data for ascertaining long term outcomes and facilitating the identification of cases for research. The post holder will be actively involved in the research, development and validation of bioinformatics solutions. They will primarily work with next generation sequencing data from short (Illumina) and long read (Nanopore) sequencing platforms, along with other applications applicable to analysing cfDNA such as digital droplet PCR. The post holder will be expected to work with the Clinical Bioinformatics team and Translational Scientists to assist the transition of new methods from research to clinical diagnostics service. The successful candidate will contribute to publications arising from the work, and will present at national and international meetings as required. The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Daycare Unit in Kingston Hospital. At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do. At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements. For further information on this role, please see the attached detailed Job Description and Person Specification To develop novel tools and pipelines for the analysis and interpretation of NGS data in the setting of early diagnosis Contribute to the development of ctDNA analysis pipelines Maintain internal databases, linked to the main public genome databases and North Thames Genomic Laboratory Hub (NT-GLH) central database To organise, store and backup data in a timely manner. To operate pipelines for the processing and analysis of raw data from high throughput sequencing (next generation sequencing) including calling of variants, translocations, amplification, deletions and other clinically relevant genomic alterations. To work with the bioinformatics team to develop automated workflows for large scale Next Generation Sequencing panels
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