Staff Scientist
Healthcare
StaffScientist-iPSCgeneticmanipulation
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Staff Scientist - iPSC genetic manipulation at Staff Scientist. Skills: iPSC genetic manipulation, CRISPR editing, Stem cell culture. Generate genotypes of interest. Differentiate iPSC lines”
Industry & Context.
Troubleshoot
What They're Looking For.
Must Have
PhD in relevant wet-lab subject, Post-doctoral experience, Experience using CRISPR editing tools, Comprehensive understanding of CRISPR-based genetic screening, Comprehensive understanding of stem cell culture, Comprehensive understanding of differentiation, Practical experience in mammalian ES or iPS, Ability to test new approaches, Ability to implement new approaches, Ability to troubleshoot new approaches, Ability to work effectively within a team, Ability to be independent, Ability to be organised, Good attention to detail, Good record keeping, Ability to lead others, Ability to inspire others
Nice to Have
Experience working with CRISPR manipulation of iPSC lines
What You'll Do.
Generate genotypes of interest
Differentiate iPSC lines
Characterise cell behaviour
Design complex culture systems
Execute complex culture systems
Collaborate with computational members
Collaborate with other teams
Contribute to supervision of students
How You'll Work.
Team & Collaboration
Computational members; Other teams within Institute; Supervise students
Communication Scope
Excellent communication
Full Job Description
Do you want to help us improve human health and understand life on Earth? Make your mark by shaping the future to enable or deliver life-changing science to solve some of humanity’s greatest challenges. **The Opportunity:** The [Cellular Genomics Programme](https://www.sanger.ac.uk/programme/cellular-genomics/) is seeking a highly motivated staff scientist to lead wet lab work in the [Lee-Six group](https://www.sanger.ac.uk/group/lee-six-group/). The group is focused on studying the earliest stages of childhood cancer by investigating the conditions under which cells with particular cancer-driving mutations gain a selective advantage over their healthy neighbours. The applicant will have the opportunity to be embedded in a large community of experimental and computational scientists with access to world-leading computational and experimental facilities at the institute. **About the Team:** Henry Lee-Six is a paediatric pathology registrar. His previous work has been focused on somatic mutations in normal tissues. He is starting a new group in the Cellular Genomics Programme with the aim of understanding the interplay of somatic mutations and development in childhood cancer. A major goal of the group is to investigate the relative contribution of mutation identity, cell state, and microenvironmental context in determining whether a mutant cell progresses to form a tumour. The group pursues this line of research by studying samples of children’s tumours and normal tissues with cutting-edge spatial transcriptomic platforms coupled to different mutation-calling technologies such as laser capture microdissection and duplex sequencing. These data are used to build models of what determines a cell’s selective advantage, which are in turn queried to suggest perturbations to a cell’s state or microenvironment that might change the relative fitness of a mutant clone. These _in silico_ predictions are then tested _in vitro_ using iPSC and cell-line models. The group is a mixtu
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