Scientist - Molecular Validation
Listed on 2026-07-18
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Research/Development
Research Scientist, Biotech Research, Drug Discovery, Immunology Research
Enara Bio is shining a light on Dark Antigen® and T-cell biology to develop cancer immunotherapies designed to improve treatment outcomes for broad populations of cancer patients with solid tumors. Our pioneering EDAPT® platform enables us to discover cancer-specific antigens, including HLA-presented and cell surface antigens, from previously uncharted genomic ‘dark matter’. The result is a growing library of Dark Antigens that can address the need for novel, cancer-specific targets in solid tumors.
Through our proprietary EnTiCE® platform, Enara is developing novel bispecific T cell engagers against Dark Antigen targets that are highly prevalent and homogenously expressed across solid tumors.
Based in Oxford, UK, Enara Bio is backed by a strong syndicate of life science investors including RA Capital, Pfizer Ventures, M Ventures, Samsara Bio Capital, SV Health Investors, and the Francis Crick Institute.
Role OverviewWe are seeking a Scientist to join our Molecular Validation team on a fixed-term basis to provide maternity cover and additional laboratory capacity during a period of increased activity and team absences.
The role will support target validation activities across Discovery and Preclinical programmes, with a particular focus on molecular and tissue-based techniques including in situ hybridisation (ISH), immunohistochemistry (IHC), immunofluorescence (IF), support RT-qPCR and related molecular biology approaches. The successful candidate will work closely with scientists across Discovery, Translational Research and Product Pipeline teams to ensure delivery of key programme milestones.
Role Requirements- Perform molecular validation experiments to support target discovery and development programmes.
- Conduct and optimise cell and tissue-based assays including:
- In situ hybridisation (ISH)
- Immunohistochemistry (IHC)
- Immunofluorescence (IF)
- Support RT-qPCR experiments.
- Generate, interpret and communicate high-quality scientific data.
- Support method transfer, documentation and knowledge-sharing activities.
- Troubleshoot assays and contribute to the development of novel experimental approaches.
- Maintain accurate laboratory records in accordance with company procedures.
- Collaborate with cross-functional teams to support Discovery, Preclinical and Translational objectives.
- Contribute to laboratory organisation, equipment maintenance and compliance activities.
- Support external CRO interactions and outsourcing activities where required.
- PhD in Molecular Biology, Cancer Biology, Immunology or a related life science discipline, or equivalent industrial experience.
- Experience performing and troubleshooting tissue-based assays such as ISH, IHC and/or IF.
- Experience working with human tissue samples, FFPE and/or Fresh frozen.
- Familiarity with image analysis software and statistical data analysis.
- Hands‑on laboratory experience in molecular biology techniques.
- Strong data analysis and scientific communication skills.
- Ability to work independently while contributing effectively within a multidisciplinary team.
- Excellent organisational skills and attention to detail.
- Experience in oncology, discovery or translational research.
- Knowledge of biomarker discovery or target validation workflows.
- Experience working with CROs and external collaborators.
- Previous experience in a biotechnology or pharmaceutical environment.
- Collaborative and team oriented.
- Flexible and adaptable in a fast‑paced research environment.
- Proactive problem solver with a strong scientific curiosity.
- Comfortable balancing multiple priorities and changing project needs.
- Committed to high scientific standards and data quality.
- Effective transfer and retention of key Molecular Validation knowledge during maternity leave cover.
- Continued delivery of Discovery and Preclinical programme milestones.
- High‑quality execution of molecular validation assays with minimal supervision.
- Strong partnership with internal stakeholders and effective contribution across multiple projects.
- Applications close on Friday 31 July 2026
. We review applications on a rolling…
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