Senior Clinical Fellow in Rare Disease Genomics
Location: Role to be based in the London offices at QMUL, Dawson Hall, Charterhouse Square, EC1
Duration: 1 year Fixed Term. Part-time (estimated at 3-4 days a week depending on the appointee’s availability).
Salary: According to current pay scale
Genomics England are seeking to appoint a Senior Clinical Fellow in Rare Disease Genomics. The post holder will work as part of the Chief Scientist’s and Participants’ project teams at Genomics England across a range of areas. The particular areas of focus will be to (i) provide clinical input to support the further development of the National Genomic Informatics System (NGIS), (ii) work with the NHS England Genomics Unit to develop metrics to inform service improvement test use in the new Genomic Medicine Service. The post may require some flexibility with regard to key responsibilities, due to the fast-moving nature of Genomics England’s work.
The role would be well suited to a Clinical Genetics consultant or a trainee with more than 9 months specialist training experience (at ST3+) who is interested in gaining experience in the establishment of whole genome sequencing in mainstream use in the NHS. The post would also be suitable for clinicians from other specialties with relevant experience in genomics.
There may be the opportunity to carry out a defined research project suitable for incorporation into a Masters dissertation as part of the post.
- To work as part of the Chief Scientist’s and Participants’ project teams at Genomics England across a range of tasks to deliver the 100,000 Genomes Project Rare Disease Programme.
- To provide clinical input in our work supporting further development of the National Genomic Informatic System (NGIS)
- Work with the NHS England Genomics Unit to develop metrics to inform service improvement test use in the new Genomic Medicine Service.
- To take part in core rare disease clinical activities at Genomics England including gene panel curation, refinement of clinical data models and medical case review.
- The role will involve joint working with other members of the Chief Scientist team, and Informatics and Bioinformatics teams and with NHS Genomic Medicine Centres (GMCs) and Genomic Laboratory Hubs (GLHs), NHS England and members of the Genomics England Clinical Interpretation Partnership (GeCIP).
Education & experience
- Medically qualified, with CCT in at the time of commencement of the post or have more than 9 months of relevant specialist training experience at ST3+ level.
- Experience in genomic medicine (at Consultant level or to the level of an established trainee in Clinical Genetics)
- Experience working within the NHS.
- Understanding of confidentiality, and the Data Protection Act 1998.
About Genomics England
Genomics England, a Government-owned company, was created in in 2013 to deliver the 100,000 Genomes Project to sequence whole genomes. In 2018, the Health Secretary announced the expansion of the 100,000 Genomes Project to see 1 million whole genomes sequenced by the NHS and UK Biobank in five years and an ambitious vision for genomic medicine in the NHS – with plans to sequence 5 million genomes over the next five years. Genomics England’s vision is to become the world leader in genomic medicine; at the forefront of embedding a new way of predicting, diagnosing and treating patients that will be transformative.
For more information about the organisation please see following website: https://www.genomicsengland.co.uk
Further information about the role
For informal enquiries please contact Dr Richard Scott, Clinical Lead for Rare Disease (firstname.lastname@example.org)
To apply, please click the apply button.
Closing date: Tuesday 28th May 2019