The Role: Contribute to strategic R&D projects (i.e. designing and execution). To perform studies to support oncolytic virus candidate pipeline development under GCLP. Your responsibilities will include: Presenting research findings/data at meetings. Prioritisation and coordination of scientific work streams and processes. Act as independent scientist reviewer and sign off lab books, verifying the calculations, and approving SOPs.
Your Background: PhD or equivalent in Molecular Biology, Virology. Experienced in cell culture, virus handling/purifications and cellular assay development. Expertise in design and execution of molecular biology based experiments (e.g. DNA/RNA extraction, PCR, cloning, gibson assembly, sequencing, transfections). Hands on execution of omics experiments (e.g. short-read/long-read sequencing, transcriptomics, primer/probe design). In-vivo oncology experience would be advantageous. Experience working with oncolytic viruses or adenoviruses (DESIRABLE). Experience of Prime Flow, RNAscope or single cell sequencing would be useful.
Benefits: Bonus Pension Private Medical Insurance Flexible working hours
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
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