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Opportunity: Cancer Genomics Data Scientist @ A life sciences company -- London, UK
Submitted by Eugene McDaid; posted on Wednesday, October 13, 2021
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DESCRIPTION
Genomics Data Scientists investigate and develop solutions to extract more information from the genome (alignment and variant calling) and to interpret the genome in the context of a persons clinical features.
They work as part of squads building and translating state of the art analytics into clinically-fit production quality solutions.
Key Accountabilities Include:
- Benchmarking and fine-tuning tools for quality control, processing and analysis of whole genome sequence data, e.g., alignment, variant callers for types of variants
- Develop algorithms for variant prioritisation / classification to improve their diagnostic potential or actionability
- Performing custom computational analysis for a range of projects in rare disease/germline or cancer/somatic samples and carefully document results using reproducible computing principles
- Developing, prototyping, and validating new features for genome analysis in collaboration with internal and external stakeholders
- Work with other squad members to ensure that solutions are implemented in a robust, scalable, fit for clinic, accredited, production ready for converting prototypes to production pipelines
- Continuously scan the scientific literature to identify new approaches to genome analysis that can be implemented to improve our capabilities
- Contribute to the publication and dissemination of our learnings in the form of scientific papers, white papers, conferences, etc.
- Establishing general bioinformatics resources for day-to-day use by colleagues
- Know and understand the meaning behind our virtues of Empathy, Integrity, Focus, Connection, Speed, Curiosity, Impact and embody them in all aspects of your role
REQUIREMENTS
Key Skills Include:
- Excellent knowledge in cancer genomics, approaches to call somatic variation and interpret cancer genomes
- Strong knowledge of statistics and/or machine learning
- Strong knowledge of high throughput sequencing algorithms and available resources. Experience with full cycle of analysing NGS data from sequencing QC to annotation and prioritization of variants.
- Strong programming skills (Python, R)
- Excellent technical writing skills
- A decent publication record demonstrating their ability to conceive and carry to conclusion scientific investigations
- Excellent ability to represent and visualise data to derive insights
- A demonstrable ability to cope under pressure and deliver to deadlines
- Experience in handling large data sets
- Ability to communicate effectively within a multidisciplinary team
- Flexible and co-operative approach to colleagues
- Experience and flexibility to collaborate on code with others including good working knowledge of Git
- Ability to work independently and to show initiative within a team
- Ability to prioritise and balance competing demands
COMPENSATION
There are some great benefits on offer with this role including a competitive salary, pension, generous holidays and more.
HOW TO APPLY
Please do not hesitate to contact Harvey Uppal at huppal[at]pararecruit.com or call (+44) 121 616 3407 to discuss this opportunity further.
Keywords: Rare, Disease, Analyst, Cancer, WGS, WES, Genomics, Bioinformatics, Germline, Somatic, Mutations, Clinical, Python, Pipelines, Statistics, Testing, Writing, Variants, Alignment, Statistical, Genetics, NGS, London
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