We are currently seeking highly motivated and talented POSTDOCS and RESEARCH FELLOWS to join our group working on the use of CRISPR and viral vectors to develop novel gene therapy technologies and strategies to treat genetic diseases. If you like responsibilities and want to take part of this wonderful adventure with a team built with deep expertise in gene therapy development, do not hesitate to contact me!
*Description*
Our laboratory focuses on developing effective and safe genome editing and gene therapy strategies for the treatment of human diseases. We follow three main complementary axes:
1) development of novel CRISPR/Cas9 tools (nickase, prime editing, etc…) and novel delivery system for CRISPR/Cas9 and donor DNA (AAV, LV, RNP, etc…);
2) assessing genome editing outcomes & genotoxicity using LRS, Guide-seq, imaging, etc…
3) development of novel treatment for genetic diseases (hemoglobinopathies, lysosomal storage disorders, muscular dystrophies)
The team is part of the UMR_951, sponsored by Genethon, Inserm and Univ. of Evry Val d’Essone (Paris Saclay) (https://integrare-umrs951.jimdo.com/home/labs/gene-editing/).
*Requirements*
First and foremost, the desire to make an impact in the field of Gene Therapy in a friendly, enthusiastic, dedicated and collaborative manner.
Candidates should be able to work independently and interactively in a team setting, be responsible, organized and have a great work capacity and enthusiasm for research and smiling and positive attitude.
Tagged as: Life Sciences
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